Typical Accountabilities: Ensures the processes for Study Delivery are executed through the development of study reports tools, facilitation of the study delivery system and maintenance of the system. As an expert, ensures delivery of a centrally managed study management service across clinical studies from start up to reporting Serve as main contact and works closely with the Document Management group until the Clinical Study Report is finalised Initiates and maintains production of study documents, ensuring template and version compliance Creates or imports clinical-regulatory documents into the Global Electronic Library according to the Global Document List Interfaces with Data Management Centre or Data Management Enablement representatives to facilitate the delivery of study related documents Manages and coordinates tracking of study materials and equipment Monitors administrative tasks during the study process, audits and regulatory inspections, according to company policies Acts as a technical owner within Patient Safety with a deep understanding of processes and internal regulations Keeps own knowledge of best practices and new relevant developments up to date Liaises with compliance team members to improve regulatory processes within the team Identifies opportunities to improve the methodology and provide practical solutions for clinical development Typical People Management Responsibility (direct / indirect reports): Approximate number of people managed in total (all levels) - None What is the global remit? (how many countries will the role operate in?): Own country Education, Qualifications, Skills and Experience: Essential: Bachelor’s degree in relevant discipline; Experience of Study Management within a pharmaceutical or clinical background; Knowledge of relevant legislation and new developments in the area of Clinical Development and Study Management Desirable: Advanced degree within the field; Professional certification; Understanding of multiple aspects within Study Management Key Relationship to reach solutions: Internal (to AZ or team): Study management function; Other AstraZeneca employees External (to AZ): External service providers and regulatory bodies Show more Show less

Job Title: Training Manager - Global Business Services Career Level - D Introduction to role AstraZeneca (AZ) has a bold aspiration to improve the lives of 200 million patients by delivering 20 new medicines by 2030. The Training Manager role is critical in giving to AZ’s long-term ambition. Global Business Services (GBS) is growing to support critical functions across the entire enterprise, and this role will be specifically focused on defining and delivering GBS opportunities within the R&D areas of the business. The successful candidate will be responsible for developing, implementing, and handling core training programs to enhance skills, performance, and productivity across our Global Patient Safety Services. This role forms part of our Central Services Team based in our Bangalore Hub. Accountabilities Training Programme Development Design, develop, and implement training programmes tailored to GBS and client goals and employee needs Create engaging training materials, specifically for GBS induction, including manuals, e-learning modules, and workshops Continuously evaluate the GBS training effectiveness and make improvements based on feedback Employee Development & Skills Enhancement Identify skills gaps and develop strategies to enhance employee competencies Work with Regional and local MC L&D resource to ensure GBS employees maintain relevant competencies to support our client’s needs Organise onboarding programmes for new hires to ensure a smooth transition into the company Training Delivery & Coordination Coordinate GBS employees’ relevant, and ongoing training content and sessions in collaboration with client L&D trainers Conduct training sessions in-person, online or through a blended learning approach Work with subject matter experts to ensure accuracy and relevance of existing and future training content Performance Evaluation & Compliance Assess training impact through feedback, assessments, and key performance indicators (KPIs) Ensure all training programmes follow industry regulations and company policies Keep up to date with standard methodologies in corporate training and learning technologies Ensure all GBS Patient Safety colleagues complete all mandatory training on time and to required standard Sustainability and Training Quality Assurance Audit and review training materials for accuracy, relevance, and compliance with industry and the client’s standards Maintain training content integrity and ensure long-term learning effectiveness Maintain accurate records of training and training completion for quality management and audit purposes Lead the GBS Patient Safety Training Centre of Excellence (CoE) through sharing best practice and proactively promoting learning and development opportunities Support the GBS Leadership Team in projects and initiatives to help the Business achieve goals and objectives Essential Skills/Experience Bachelor's degree in human resources, Business Administration, education or a related field 3+ years of experience in training, learning and development, or human resources Strong presentation skills and effective delivery of L&D practices Cross functional collaborative approach Effective and analytical thinking with the ability to measure and assess the effectiveness of training initiatives Problem solving Excellent attention to detail Excellent written and verbal communication skills Desirable Skills/Experience Experience in corporate training, instructional design, or leadership development Experience in Pharmacovigilance, Patient Safety or similar industry Influencing, and Conflict Resolution skills. Successful participation in above-market projects Familiarity with Learning Management Systems and e-learning tools When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Join us at AstraZeneca where you can combine technology skills with a scientific mindset while broadening your understanding of our wider work. We empower the business to perform at its peak by delivering world-class technology and data solutions. Our work unlocks the potential of science, optimizing AstraZeneca by maximizing efficiencies and finding new ways to drive productivity. With investment behind us, there's no slowing us down. There's no better place to make a big impact. Ready to make a difference? Apply now! Show more Show less

Job Title: Quality & Compliance Manager - Global Business Services Career Level - D Introduction to role AstraZeneca (AZ) has a bold aspiration to improve the lives of 200 million patients by delivering 20 new medicines by 2030. This role is critical in contributing to AZ’s long-term ambition. Global Business Services (GBS) is growing to support critical functions across the whole enterprise. This role will be specifically focused on defining and delivering GBS opportunities within the R&D areas of the business. GBS is enhancing its customer focus by establishing Research & Development (R&D) Services to improve alignment and strengthen our relationships with SET areas. R&D Services is a key element of the GBS Bold Ambition, driving our vision to enable AstraZeneca to change and grow at speed. Between now and 2030, 10 new R&D capabilities are to be established, ensuring that GBS can offer the broad range of services required to support AZ ambitions. As the Patient Safety Quality Manager, you will be responsible for developing and maintaining excellence in global PV Quality, Compliance, Audit and Inspection management, Process Improvement, and Data Governance. You will ensure oversight of the PV Quality Management System, maintain inspection readiness, and ensure compliance with worldwide pharmacovigilance regulations. Collaborating with key PV and non-PV stakeholders across AstraZeneca, you will align with company-wide standards, oversee compliance and quality of PV processes, conduct internal audits and deviation investigations, analyse and report on key metrics, and support the client’s continuous improvement plans to establish best-in-class PV practices. This role is crucial in ensuring the timely and accurate quality and compliance from our Bangalore hub, contributing to AZ’s overall global pharmacovigilance efforts and ultimately supporting patient safety worldwide. Accountabilities Oversee the daily operations of Quality and Compliance within the Bangalore hub, supporting the efficient processing and reporting of adverse event cases within regulatory timelines Lead and manage the Quality and Compliance Advisors, ensuring appropriate guidance, training, and performance management to maintain high-quality standards Implement and maintain standardised operating procedures (SOPs) for case intake and processing, ensuring consistency with global pharmacovigilance practices Collaborate with other GBS Patient Safety Hub Managers and Directors and the Global Patient Safety (GPS) team to improve processes and share standard methodologies Control the tools to monitor compliance, quality metrics, and key performance indicators (KPIs) for global PV processes, license partners, and vendors. Ensure feedback and trend analysis to support AstraZeneca continuous improvement. Lead internal assessments, support external audits and regulatory inspections, and implement standard processes for audit and inspection management in collaboration with the client’s Quality Assurance teams. Oversee Corrective & Preventive Actions and deviation processes, provide support and guidance on development and implementation, track progress, collect evidence, and coordinate effectiveness checks. Support a drive in continuous process improvements by analysing audit/inspection findings, identifying quality risks, and leading initiatives to enhance PV compliance and operational efficiency. Develop and maintain internal training programs related to audit/inspection readiness, compliance, and quality performance indicators, ensuring alignment across global PV teams and affiliates. Support data governance initiatives to ensure high-quality data for decision-making, assess downstream implications of data activities, and align ongoing initiatives with compliance requirements. Ensure compliance with global regulatory requirements, including timely submission of appropriate Regulatory Reports to relevant authorities Serve as a subject matter expert during audits and inspections related to case intake processes within the hub Contribute to the development and optimisation global patient safety processes, systems and tools, including automation solutions Stay updated on regional and global pharmacovigilance regulations for those MCs supported by the hub, ensuring that necessary changes are implemented to maintain compliance Maintain appropriate staffing levels in the hub, being responsible for recruitment of new staff where required. Ensure that training and development of GBS PS staff results in consistent and compliant knowledge and skills within the hub. Essential Skills/Experience BA or BS degree or equivalent Extensive experience in the pharmaceutical, biotechnology, or related industry. Strong background in Pharmacovigilance, Regulatory Affairs, or Safety Quality Assurance, with expertise in establishing safety quality system standards that impact multiple departments and management levels. Proven experience in people or project management within a highly matrixed, multicultural global setting, demonstrating facilitation, negotiation, problem-solving, and conflict resolution skills. Deep knowledge of global safety regulations for both marketed and investigational products, along with expertise in process management, standards, training, and IT functions across the pharmaceutical product life cycle. Solid understanding of PV and Clinical Research processes, including their interfaces and contributions to the overall PV system. Expertise in Pharmacovigilance, data management, and adverse event reporting and processing, with proficiency in relevant software tools Exceptional attention to detail and commitment to maintaining high-quality standards in case processing and reporting Ability to work in a fast-paced environment, manage multiple priorities, and meet tight deadlines Strong analytical and problem-solving skills, Excellent communication skills, both written and verbal, with the ability to interact effectively with internal and external stakeholders across different regions Ability to work in a team environment / works collaboratively Desirable Skills/Experience Knowledge of global and regional pharmacovigilance regulations Track record in managing and optimising Patient Safety processes Proficiency in safety databases, ideally Argus, and case management systems When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. AstraZeneca is a place where technology meets science to create life-changing medicines. We empower our teams to innovate using cutting-edge technology platforms combined with data analytics. Our collaborative environment fosters creativity as we work together to push boundaries. With significant investment behind us, we are driving cross-company change that disrupts the industry. Ready to make an impact? Apply now! Show more Show less

Title : Director - Business Process Management GCL : F Introduction to role: Do you have expertise in, and a passion for, improving the way we run our business through excellent process management? Would you like to apply your expertise to impact the delivery of major capital projects within AstraZeneca ? Our Global Engineering (GE) team is at the forefront of innovation, establishing cutting-edge facilities worldwide where AstraZeneca advances science to deliver life-changing medicines. We scope, plan, and execute major capital projects across our Operations sites, ensuring maximum business lifecycle benefits. We also provide strategic advice, helping the business make informed asset decisions while integrating the latest technology. Sustainability is embedded in our work as part of AstraZeneca’s Ambition Zero Carbon initiative. Join us in driving change and shaping the future! Accountabilities: As the Global Engineering Business Process Management (BPM) Lead you will be driving the process excellence strategy and representing the function in global networks. Inspire and drive change by engaging with process users, business leaders, and partners to embed a process-centric culture across Global Engineering and the enterprise. A key remit of the role is being the Business Process Owner (BPO) for the AZ Capital Project Delivery Process (CPDP). You will lead a process network team with skilled individuals from various regions and functions within GE. Your mission? To enhance capital project delivery on time, quality, and cost using BPM approaches and innovative digital technology. Also, as our Chennai Tower Lead, you'll play a pivotal role in establishing GE's presence in Chennai, setting up the team, and driving culture through your leadership. Other responsibilities include: Drive standardization, simplification, and continuous improvement in the CPDP process and related sub-processes enabling the effective and efficient delivery of a Global Portfolio of Major Capital Projects. Lead the development of process capability and culture across GE through BPM and Lean principles. Establish a digital strategy for CPDP, incorporating new technology/digital tools to enhance performance and user experience. Set strategic direction for CPDP in collaboration with the Executive Process Owner. Define key metrics; monitor and improve performance for Major Capital Projects. Participate in project assessments and evaluations during stage gate reviews of capital projects. Manage relationships with key partners, both internal and external. Essential Skills/Experience: Proven track record of shaping and developing innovative solutions with significant impact within the business area or organization. Strong leadership skills, experience from leading in a matrix organizational set-up. Demonstrated application of behavioral, cultural, and business change methodologies in driving multi-functional improvement initiatives. Excellent verbal and written communication and relationship-building skills with experience collaborating and sharing knowledge between global teams. Outstanding influencing, listening, and coaching skills; ability to communicate with and influence all levels of the organization. Educated to undergraduate degree level or higher in a technical or business field. Desirable Skills/Experience: Experience in program/project management with a consistent track record is advantageous. Experience working in a global organization with complex/geographical context is beneficial. Lean and BPM experience is crucial for success in this role. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, you'll find a strong connection to patients that drives us every day. United behind one mission—finding the best solution to put our patients first—you'll play a critical role in delivering innovative medicines until they reach those who need them most. With constant new products and launches, there's never been a better time to join us and shape our future with a significant contribution to life-changing medicines. Ready to make an impact? Apply now to join our dynamic team! Show more Show less

Job Title - SAP Enterprise Analytics Business Analyst Career Level - E We are one purpose-led global organisation. The enablers and innovators, ensuring that we can fulfil our mission to push the boundaries of science and discover and develop life-changing medicines. We take pride in working close to the cause, opening the locks to save lives, ultimately making a massive difference to the outside world. AstraZeneca (AZ) is in a period of strong growth and our employees have a united purpose to make a difference to patients around the world who need both our medicines and the ongoing developments from our science. In this journey AZ must continue to work across borders and with partners and new colleagues in a fast and seamless way. The ambition, size and complexity of the organisation, coupled with the opportunities afforded by new technology, has led the Board to approve a large-scale transformation programme – Axial. The Axial Programme will be powered by S/4HANA a new ERP (Enterprise Resource Planning) system which will be implemented right across the organisation and will provide our business with standardised processes, enhanced financial management, common data and real time reporting, transforming the way we work through our entire supply chain - from bench to patient. The new system will be used by more than 20,000 employees daily, is foundational to all AZ entities and is central to most core business processes. This is a once in a generation programme for AstraZeneca and will shape our ways of working globally for many years to come. The Axial programme needs the best talent to work in it. Whether it’s the technical skills, business understanding or change leadership, we want to ensure we have the strongest team deployed throughout. We are aiming to deliver a world class change programme that leaves all employees with a fuller understanding of their role in the end-to-end nature of our global company. This programme will provide AZ with a competitive edge, to the benefit of our employees, customers and patients. Drive innovation at AstraZeneca by delivering cutting-edge SAP analytics and AI capabilities. Collaborate with the Analytics Service Lead to design ITIL-based processes, manage ServiceNow operations, and lead continuous service improvements. We’re looking for proven service management expertise and, ideally, experience with SAP ecosystems (e.g. SAP S/4HANA , Analytics Cloud ), ITIL certification, and regulatory frameworks. Knowledge of Agile, digitization, or industries like pharma is a plus. Shape world-class customer experiences in a dynamic, global environment. Ready to make a difference? Apply now. We are looking for a business analyst who wants to shape the requirements for some of the re-used analytics artefacts on AstraZeneca’s SAP analytics stack. We are building out teams to face key finance and operations process areas. And, more importantly for this advert, we are building out an enterprise team to build and run the cross-cutting data products and dashboards. Data products like dimensions for business partner, material master, cost centre, profit centre, location and geography; or fact tables for complex multi-process reporting and exports to other data hubs. This team will be a true agile delivery team. The team will work in a transparent and agile way, meaning there will be a published roadmap of analytics products and a constant flow of new work from across the Axial program and AZ. You will be working with the engineering teams and product owners from across the SAP space to define the detailed requirements for enterprise analytics assets (both data and dashboards). We are looking for a broad range of skills so are open minded when it comes to your: Desirable skills, knowledge and experience: Business analysis for analytics, Visualisation best practices, Data warehousing, Data modelling, Requirements gathering, Data analysis, Systems analysis, Finance and Operations processes (e.g. R2R, P2P, O2C, Network and Supply Chain, Production), Work in a regulated environment such as GxP or SOx, Master Data. Why AstraZeneca? At Astrazeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. So, what’s next? Are you already imaging yourself joining our team? Good, because we can’t wait to hear from you. Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and hope its yours If you’re curious to know more then we welcome your application no later than Where can I find out more? Our Social Media, Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/ Follow AstraZeneca on Facebook https://www.facebook.com/astrazenecacareers/ Follow AstraZeneca on Instagram https://www.instagram.com/astrazeneca_careers/?hl=en Show more Show less

Job Title: Senior Network Reliability Engineer GCL: D2 Introduction to role: Are you ready to influence the future of network technology and drive innovation at AstraZeneca? As a Senior Network Reliability Engineer, you'll play a pivotal role in implementing, operating, and optimizing network products that are crucial to our strategic vision. Collaborate with multi-functional teams, including Cyber Security, Cloud, and Workplace Enterprise Services, to deliver durable and resilient network services. Join us in a Scaled Agile operating model and be part of a team that accelerates change and enhances the client experience. Accountabilities: In collaboration with partners, ensure technology-based solutions are supported by the right architectures, systems, and operating models. Drive projects, operations, optimization, automation, and security within Network Services. Partner with cross-technology teams to innovate and deploy Next Gen Wireless Network, LAN/WAN, Cloud, Security, and collaboration technology solutions. Understand evolving work trends in design, engineering, and modeling applications to support network infrastructure. Participate in a NetDevOps operating model to expedite change delivery. Engage in service improvement activities and ensure accurate completion. Essential Skills/Experience: Own network implementation, operations, reliability and processes, crafting the crucial link between AZ strategic vision into Network solution engineering. Proficiency in one or more technology domains, may be cross-domain expert to able to solve complex and critically important problems within a business or across the firm. Perform regular audits to identify and remediate network risks or issues proactively. Evaluate all business requirements and identify solutions how the different elements of business, information, and technology can be applied to solve a specific problem. Influence portfolio investments for key technology solutions in line with our strategic roadmaps. Ensure network operational support at scale for Block, Object and File both on-prem and in the public cloud. Work with automation team to design, code, test and deliver software to automate repetitive and manual operational work. Solve priority incidents, engage and facilitate blameless postmortems and ensure permanent closure of incidents. Help develop software for reliability and scale, ensuring minimal refactoring or changes. Successful execution of infrastructure weekend changes in product and environment. Identify gaps between applicable requirements and current procedures/controls, Drive resolution of mitigating controls. Develop and implement solutions that strengthen business operating models, enhance the client experience, and improve efficiency and controls. Work with business partners to design and implement enhancements to existing processes and/or business applications, introduce new processes and/or toolsets, and engage in process re-engineering. Expertise in preparing high quality CRD, HLD and LLD design documents. Experience in sequencing the activities, scheduling the tasks, and preparing project plan. Experience in planning and conducting vigorous wireless network tests and generating a detailed test reports from performance, security, scale and resiliency point of view. Design and implementation of wireless solution in multi-tenant environment. Good knowledge on public cloud connectivity Cloud exchange, direct connect, Express route to Public Cloud provides. Desirable Skills/Experience: CCIE/CCNP or equivalent certification with Minimum 10 years of relevant working experience, with the last 5 years in large-scale network architecture design implement and support network deployment, implementation, and operations. TOGAF or equivalent and ITIL certifications are added advantage. Excellent communications skills, with the ability to explain complex technological ideas and concepts in a way that is understandable to a non-technical audience. Ability to analyze and resolve project-related issues. Ability to work in a high paced environment, be flexible, follow tight deadlines, organize, and prioritize work. Significant experience working with vendors, professional services, and providers. Automation first attitude. Must have in-depth and technical hands-on experience in one or more of the following capabilities SD-WAN, Wireless, Network Security, DC, Cloud Networking or Network Automation. Strong technical knowledge in high availability design, implementation, optimization, and operations. Candidate with large enterprise working experience is an added advantage. Agile Enterprise mentality. Self-starter who continuously develops new skills and proactively leads own career and development. Excellent influencing, networking, and collaborative working skills. Ability to work well in and lead/collaborate across diverse matrixed global teams. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, our work directly impacts patients by transforming our ability to develop life-changing medicines. We empower our teams with ground breaking science combined with leading digital technology platforms. With a passion for data analytics, AI, machine learning, and more, we drive cross-company change to disrupt the industry. Here you can innovate freely while being supported by a diverse team committed to making a meaningful impact. Ready to make a difference? Apply now to join us on this exciting journey! Show more Show less

Job Title: Analytics and Reporting (A&R) – Biometrics Dev Ops Lead Career Level: E Introduction to role Are you prepared to apply your expertise in biometrics and DevOps to make a real impact? As an A&R Biometrics DevOps Lead, you will be a key member of the A&R Product IT DevOps team, managing core A&R applications such as Entimice and SAS GRID. Collaborate with Platform Managers, Product Managers/Owners, Senior Platform Engineers, Release Managers, and Solution/Integration Architects to establish standard processes in software development, business analysis, solution design, enterprise software integration, and project management within the BizDevOps IT Platform Delivery Model. Accountabilities Collaborate with vendors and internal collaborators to define requirements and develop implementation plans. Monitor system change requests and ensure alignment to IT standards. Serve as Technical Subject Matter Expert (SME) for SAS-related applications. Provide guidance and assist in the preparation of system-related specifications and documentation. Maintain day-to-day application systems, identifying and solving issues. Ensure all production changes align with life-cycle methodology and risk guidelines. Work on application enhancements and upgrades as vital. Liaise with internal teams/vendors to address application issues. Communicate effectively with users during planned/unplanned outages. Follow good documentation practices by creating and publishing Knowledge Base Articles (KBAs). Create technical backlogs/Story/Epic in JIRA based on product priority. Essential Skills/Experience Biometrics (A&R) Domain/Technology Bachelor or master’s degree in computer science or life science related field with IT/CRO/Pharma experience with a total of 15 years of experience. Industry experience working or implementing solutions based on CDISC Clinical Reporting Standards (SDTM, AdaM, TLF Reporting). Minimum 7-8 years working experience in SAS GRID related administration. Accredited Certifications SAS Administration from Vendor. Good understanding of SAS Programming & shell scripting, reporting tools, infrastructure. Ensure system security and control procedures are implemented and maintained. Maintain configuration specification documentation for functional and integration configuration. Work with software vendors on product requirements and issues related to the platform. Knowledge of client-server networking and database management. Administration background in SAS Viya 3.5/4.0 environments. Experience with SAS Visual Analytics & Power BI highly preferred. Familiarity with shell scripting & groovy scripting. Experience in R and Python is an added advantage. End-to-end knowledge of clinical trial development processes and associated system landscape. Solid grasp of common industry standard business practices related to clinical trials. Strong knowledge of ICH/G guidelines, 21 CFR Part 11, clinical trial methodology, and software development lifecycle activities. Knowledge of support processes like Incident Management, Problem Management, Change Management. Knowledge or experience with JMP Clinical, JReview, StatXact, CR Toolkit, Pinnacle 21. IT Engineering: Expertise and engineering attitude to help design and implement Clinical Data Solutions adhering to Products on Platform Strategy. Demonstrable ability to handle diverse collaborators and ensure high satisfaction delivery. Ability to work independently in a dynamic environment. Good communication and interpersonal skills to lead customers in urgent situations. Experience in Gxp validated systems implementation and maintenance of applications. Knowledge of Identity management solutions based on AZURE, OKTA, Oauth, Ping Federate/AD technologies. Understanding database concepts for optimizing reporting, data mapping, and programming. Experience in developing Interfaces/Integration between on-premises and SaaS Platform enabled Products using API’s, Web Services (MuleSoft), and ETL (SnapLogic) tech enablers. Knowledge of using/creating build tools and CI/CD (maven, ant, gradle, Sonar). Experience with Cloud Platforms such as AWS, AZURE. Experience working with JIRA, Confluence, Bitbucket, Automated Testing tools. Experience working in agile teams using methodologies such as SCRUM and SAFe & leading a team of 5+ & working in an Agile DevOps model. Experience programming in Java or other object-oriented programming languages. Experience delivering or developing workshop material, training, gap analyses, or requirements gathering sessions with business and system collaborators. Certification in IT delivery framework, Scrum Master, DevOps Lead role. Participate in business requirement gathering and design activities with business & IT collaborators as part of scrum team. Perform delivery activities through Design/Build/Test/Deploy phases for regular releases on A&R platform. When we put unexpected teams in the same room, we fuel bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and daring world. At AstraZeneca, we demonstrate technology to impact patients' lives by developing life-changing medicines. We are a purpose-led global organization that pushes the boundaries of science. Our work directly impacts patients by redefining our ability to develop life-changing medicines. We empower our business to perform at its peak by combining ground breaking science with leading digital technology platforms and data. Join us at a crucial stage of our journey to become a digital and data-led enterprise. Here you can innovate, take ownership, experiment with groundbreaking technology, and solve challenges that have never been addressed before. Ready to make a difference? Apply now! Show more Show less

Job Title: Director – Patient Platform Engineering GCL- F About Commercial IT Commercial IT is a global IT capability supporting the Commercial organisation. We business partner with Commercial areas: Biopharma, Oncology, International and Japan – and also Rare Disease Unit. We operate out of hubs sites including in the UK, Sweden, US and out of our Global Innovation Technology Centres in India and Mexico – and in markets all over the world. Here our work has a direct impact on patients – transforming our ability to develop life-changing medicines. We empower the business to perform at its peak and lead a new way of working, combining cutting-edge science with leading digital technology platforms and data. All with a passion to impact lives through data, analytics, AI, machine learning and more. Introduction to role: Are you ready to lead the charge in transforming patient platforms and associated technologies? As the Director of Commercial IT – Platform Engineering, you'll be at the forefront of innovation, overseeing the end-to-end ownership and accountability of solutioning, design, development, execution, and operational management of production. Dive into technologies like Salesforce Communities, Health Cloud, AgentForce, Einstein, Salesforce Voice over AWS, and AppExchange implementations. Collaborate across engineering roles, testing capabilities, and business units while working closely with third-party suppliers to drive success. Accountabilities: Maintain deep working knowledge of platforms/products/infrastructure aligned with our global estate (US, ROW: LATAM, AsiaPAC, ANZ, Europe & Middle East) Lead build, test, and deployment activities for assigned platform and IT product initiatives Serve as the voice of technical expertise to peers and 3rd party development suppliers ensuring alignment to AZ IT and Commercial IT standards Oversee platform engineering resources to validate business and functional requirements Act as an internal consultant on key assigned platforms and technologies for IT and business partners Evaluate new technologies/application features and recommend strategic roadmaps through prototyping Refine business requirements, set priorities, resolve issues, and deliver innovative solutions Collaborate with regional solution architects and capability teams to co-create functionalities with strategic markets Demonstrate understanding of AstraZeneca’s application development processes – handle CI/CD pipelines and DevOps WOW Lead, mentor, and coach the AZ Application Development team globally to enhance throughput and quality Drive alignment with cyber security standard processes ensuring platform security Continuous Improvement and Innovation: Partner with Platform Success Lead(s) on continuous improvement opportunities within platform/product backlogs Identify new hardware/software technologies for specialized business needs Identify process issues and implement changes to improve IT efficiency Essential Skills/Experience: Understanding of the Salesforce technology stack – Salesforce Health Cloud, Salesforce Voice, Salesforce Communities mandatory Understanding and use integration patterns – experience designing, implementing MuleSoft mandatory Consistent record of crafting and operating critical applications Experience working with and influencing business and BA’s around Salesforce architecture and designs Experience supporting and guiding development teams Expertise in application design patterns and processes Prior experience in an Information Services/Information Technology environment with good eye for business including SaaS & professional services contract management Expertise in Continuous Integration and Deployment methods delivered as part of an agile team Minimum bachelor's degree and engineering experience Desirable Skills/Experience: Einstein 1, AgentForce, and Voice AI experience At AstraZeneca, we are passionate about making a meaningful impact on patients' lives. Our work combines cutting-edge science with leading digital technology platforms to empower the business to perform at its peak. We foster an environment where curiosity to learn, grow, and develop is at the heart of what we do. With a dedication to innovation and a spirit of experimentation, we offer countless opportunities to explore new technologies and transform the roles of colleagues. Join us in a dynamic environment where your personal and professional journey is filled with unlimited potential. Ready to take the next step in your career? Apply now to join our team! Show more Show less

About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. Job Description / Capsule Field based scientific experts in assigned therapeutic area that is responsible in the execution of the Medical Affairs Plan(s) for pre-launch and/or newly launched products/indications. Shapes clinical practice through scientific engagements, partnerships and collaborations with traditional (e.g Specialist KEEs for MSLs & Primary Care Physicians for CSLs), and where appropriate non-traditional (e.g. policy and decision makers, PAGs, government, innovative solution providers) experts, as well as, with internal stakeholders to drive enhanced patient outcomes and the safe and effective use of AstraZeneca medicines. Developing and enhancing professional relationships and partnerships with healthcare professionals and other healthcare ecosystem stakeholders according to the Integrated Engagement Plan. Provides scientific, technical, and pharmaco- economic information to HCPs and key stakeholders through one-on-one discussions and medically lead meetings as experts and confidence generation activities. Can be involved and may lead evidence generation activities as part of the implementation of the medical strategy. Acts as catalysts, with a deep understanding of the health system (environment, priorities, clinical pathways, patient journeys) and its challenges, to gather insights and execute according to the medical strategic plans to deliver strategic, scalable & sustainable clinical practice transformations, enhancing access to equitable quality care for patients and enabling the adoption of our innovative medicines. Scientific Expertise: Maintain clinical/scientific expertise in disease state management, AstraZeneca products, emerging therapies, and the competitive landscape. Contribute to the development and provide project leadership/ management of the therapeutic area Field Medical Strategic Plan (FMSP). Act as a subject matter expert/resource for internal and external stakeholders. Work with internal stakeholders in the development and delivery of appropriate training and mentoring needs within therapeutic area. Scientific Exchange: Engage in peer-to-peer level dialogue with key customers and deliver appropriate clinical/scientific content through utilising the correct channel mix, which will differentiate AstraZeneca products from those of other companies. Respond to unsolicited customer inquiries and provide focused and balanced clinical / scientific information that supports the safe and appropriate use of AstraZeneca’s products and services. Provide scientific/clinical support and deliver presentations to internal and external stakeholders. Identify and establish relationships with key customers and other scientific thought leaders for engaging them in ongoing scientific dialogue on AstraZeneca products and unsolicited discussions about compounds in development. Organize and facilitate scientific events such as MSL events, Symposiums, Scientific Exchanges, Advisory Boards/Expert Panels, non-promotional standalone events, Meet the Professor sessions, etc., with KEEs and HCPs. Prioritize these events based on their relevance in the patient journey for the related disease. Deliver informative lectures at scientific events tailored to healthcare professionals, aligning with the field medical. Customer Insight: Effectively identify, gather, analyse, synthesise, report and forward relevant new knowledge about the external scientific/medical environments to internal stakeholders Provide internal stakeholders with actionable items related to medical / product strategy or clinical development based on customer perspectives. Partner with traditional and non-traditional stakeholders to identify gaps in the patient experience journey as insights to be included in the medical / product strategies. Strategic Relationship: Develop peer-level relationships with medical and scientific experts, including Healthcare Professionals and collaborate with other internal teams for other key external stakeholders (e.g. policy and decision makers, PAGs, government, innovative solution providers) consistent with Medical objectives. Identify pre-clinical, clinical, and post-marketing study investigators in alignment with Medical Plans. Support data generation activities including participating in reviews of Investigator sponsored studies. Looks to broaden the My MA contact list where appropriate to include non-traditional KEEs from government, payer groups, researchers and clinical advisors who may support practice change initiatives. Establish win-win partnerships with traditional and non-traditional stakeholders to deliver on strategic, scalable and sustainable solutions addressing patient healthcare access gaps within the ecosystem. Other: Responsible for leveraging digital and innovation / technology as enablers for scientific exchange and creating patient centric solutions. Possesses a solid grasp of pharmacovigilance and GxP principles, showcasing a clear understanding of their significance. This includes practical knowledge of Good Clinical Practice (GCP), various types of clinical studies, and requirements for reporting adverse events (AEs). Possesses a solid grasp of pharmacovigilance and GxP principles, showcasing a clear understanding of their significance. This includes practical knowledge of Good Clinical Practice (GCP), various types of clinical studies, and requirements for reporting adverse events (AEs). Exhibits a robust understanding of the Ethical Interactions Policy, along with relevant standards, local laws, and regulations. Moreover, possesses the ability to provide training to others in this domain. Adherence to internal processes and AstraZeneca Global Field Medical Standards and the external regulations including but not limited to clinical trials, promotional activity (e.g. Local Code of Conduct) and pharmacovigilance activities to meet internal SOP and local regulations. Essential Education, Qualifications, Skills and Experience Scientific and or a master’s degree in a scientific discipline Excellent oral and written communication and interpersonal skills Ability to communicate internally and externally using the different channel mix. Excellent project management skills Excellent presentation skills High level analytical and conceptual thinking Desirable Doctoral degree in a scientific discipline (e.g. M.D., Ph.D., Pharm.D.) Experience in pharmaceutical industry, regulatory environment, clinical or preclinical research, and knowledge of a therapeutic area disease state and treatment. Experience with basic research, drug discovery, drug development and KEE interactions. Why AstraZeneca? At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth, and development. We’re on an exciting journey to pioneer the future of healthcare. Show more Show less

Job Title: Director - Enterprise Architect Career Level - F Introduction to role In our fast-paced business environment, agility, strategy, and innovation are of utmost importance. As technology and practices progress at outstanding rates, organizations are increasingly realizing the necessity of centralized hubs dedicated to harnessing these advancements effectively. This is where the AstraZeneca Architecture Center of Enablement (ACoE) becomes crucial. As a member of AstraZeneca’s Architecture Center of Enablement, you will be responsible for delivering and maintaining components of an operating model that emphasizes the creation of reusable building blocks and ensures quality and assurance. These are imbued with standard processes, quality checks, and expert IT knowledge, facilitating self-service and efficient automated deployments across the organization. This approach aims at accelerating solution delivery. As an Enterprise Architect in AstraZeneca’s Centre of Enablement (‘CoE’), you will lead the creation, development, and governance of a CoE within the organization. The CoE will serve as the central hub for best practices, standards, and reusable assets across technology and business units, enabling accelerated innovation, improved alignment between IT and business strategies, and consistent delivery of digital transformation initiatives. You will work closely with key stakeholders, including IT leadership, business leaders, development teams, and project managers, to drive architectural consistency, streamline decision-making, and foster a culture of innovation. Your responsibility will be to ensure the enterprise architecture is scalable, secure, and flexible enough to meet the evolving needs of the business. Accountabilities Establish the Centre of Enablement CoE Framework Lead the development of an Agile framework for the CoE, focusing on creating reusable architectural patterns, tools, methodologies, and standards. Lead the development of architectural assurance and ensure that the agreed-on standards and principles are realized and adhered to. Identify key proficiencies and resources vital for the CoE to drive innovation and operational excellence. Governance and Standards Lead the definition, implementation, and maintenance of architectural best practices, frameworks, and technology standards across all business and IT functions. Lead the development and application of governance policies for the use of new technologies, ensuring adherence to architecture standards and compliance requirements. Provide oversight and mentorship to stakeholders on adhering to CoE standards and using reusable assets. Cross-Departmental Collaboration Collaborate with architects across the enterprise, product owners, and IT teams to ensure that the CoE supports the delivery of strategic objectives. Act as a bridge across business and technology domains, ensuring alignment in priorities and accelerating the deployment of key digital solutions. Facilitate communication and knowledge-sharing across teams, fostering a collaborative and innovative culture. Solution Design and Enterprise Architecture Be accountable for supporting the development of agile architecture standards, technology domain strategies, roadmaps, and blueprints templates for core focus areas. Understand implications of IT architecture requirements to ‘As-Is’ architectures and define/update ‘To-Be’ architectures applying AZ architecture guiding principles. Design and develop enterprise-wide solutions that ensure integration, scalability, security, and maintainability. Establish and manage an architectural repository of design patterns, reference models, and technology standards for future projects. Support strategic projects and initiatives by providing architecture expertise and ensuring alignment with long-term business and IT strategies. Performance Measurement and Continuous Improvement Measure and report on the CoE’s efficiency in enabling project teams and optimizing technology investments. Drive continuous improvement by gathering feedback from team members and regularly reviewing and improving CoE capabilities. Ensure the CoE operates as a centre of excellence, constantly refining methods to deliver faster, more reliable, and higher-quality solutions. Essential Skills/Experience Relevant technical degree or equivalent Demonstrated technical depth & experience in at least one technical or architectural domain. Experience influencing and/or developing solution direction and standard adoption through the use of architecture capability building blocks, strategies, and roadmaps Experience developing and leading innovative business capability definition and creation activities within one or more technical or architectural domain. Proven experience inspiring change and challenging approaches/ideas. Experience developing and handling relationships with business team members & third-party suppliers Experience working within and developing policies, procedures, and guidelines within a secure, quality, and compliance environment. Big-picture thinking, being able to consider the broader context and long-term implications of decisions or strategies Critical thinking, ability to question assumptions, weigh evidence, and consider alternative perspectives before reaching a conclusion Openness to change, willingness and ability to accept new insights, adapt to different circumstances, and support innovation Strong communication, facilitation, and relationship-building skills Awareness of developments in the marketplace and understand the relevance and potential impact to AZ IS Desirable Skills/Experience Exposure to large Justification phase work – product evaluation, argument formulation Experience working in global diverse working environments. Good business acuity Understanding of the pharmaceutical/healthcare industry and competitor activity on a particular architecture and Information Management Ability to work well in diverse, multinational teams and validated ability to influence others to achieve positive outcomes Demonstrate initiative, strong customer orientation When we put unexpected teams in the same room, we unleash ambitious thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. There's never been a better time to join Technology at AstraZeneca. We've been busy building and developing our technology which is now enabling our transformation to become a digital and data-led enterprise. There's a huge opportunity to develop, explore and thrive during our next chapter. Here our work has a direct impact on patients by redefining our ability to develop life-changing medicines. We empower the business to perform at its peak by combining pioneering science with leading digital technology platforms. Join us at this crucial stage of our journey in becoming a digital enterprise. Ready to make an impact? Apply now! Show more Show less

Job Title - SAP Enterprise Analytics Engineer Career Level - D We are one purpose-led global organisation. The enablers and innovators, ensuring that we can fulfil our mission to push the boundaries of science and discover and develop life-changing medicines. We take pride in working close to the cause, opening the locks to save lives, ultimately making a massive difference to the outside world. AstraZeneca (AZ) is in a period of strong growth and our employees have a united purpose to make a difference to patients around the world who need both our medicines and the ongoing developments from our science. In this journey AZ must continue to work across borders and with partners and new colleagues in a fast and seamless way. The ambition, size and complexity of the organisation, coupled with the opportunities afforded by new technology, has led the Board to approve a large-scale transformation programme – Axial. The Axial Programme will be powered by S/4HANA a new ERP (Enterprise Resource Planning) system which will be implemented right across the organisation and will provide our business with standardised processes, enhanced financial management, common data and real time reporting, transforming the way we work through our entire supply chain - from bench to patient. The new system will be used by more than 20,000 employees daily, is foundational to all AZ entities and is central to most core business processes. This is a once in a generation programme for AstraZeneca and will shape our ways of working globally for many years to come. The Axial programme needs the best talent to work in it. Whether it’s the technical skills, business understanding or change leadership, we want to ensure we have the strongest team deployed throughout. We are aiming to deliver a world class change programme that leaves all employees with a fuller understanding of their role in the end-to-end nature of our global company. This programme will provide AZ with a competitive edge, to the benefit of our employees, customers and patients. Join Axial as an Engineer and help build cutting-edge pipelines and visualizations on our new SAP analytics stack using Datasphere and SAP Analytics Cloud. Be part of a self-sufficient, agile team creating high-impact, reusable data products and dashboards that drive business decisions. With opportunities to work across data pipelines, modeling, testing, and more, this is your chance to shape the future of enterprise analytics while advancing your skills with world-class tools! We are looking for engineers who want to build pipelines and visualisations on the new SAP analytics stack (Datasphere and SAP Analytics Cloud). We are building out teams to face key finance and operations process areas. And, more importantly for this advert, we are building out an enterprise team to build and run the cross-cutting data products and dashboards. Data products like dimensions for business partner, material master, cost centre, profit centre, location and geography; or fact tables for complex multi-process reporting and exports to other data hubs. This team will be self-sufficient, so you will get experience of everything – data pipelines, data analysis, data modelling, testing, incident management. The team will work in a transparent and agile way, meaning there will be a published roadmap of analytics products and a constant flow of new work from across the Axial program and AZ. You will be part of a team that creates the most re-used analytics artefacts on the stack. This means you need to have a passion for well-engineered analytics. You are likely to have experience of some (but not all) of the following: ETL tooling; data modelling; SAP analytics tooling; dashboard creation; analytics best practices; data warehousing; data modelling; analytics testing; SAP data. We will provide training on SAP Datasphere and SAP Analytics cloud. Desirable experience: ETL tooling / data pipeline tools, Data modelling, SAP data and associated business processes, SAP Datasphere, SAP Analytics Cloud, Dashboard creation, Analytics best practices, Data warehousing, Analytics testing. Why AstraZeneca? At Astrazeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. So, what’s next? Are you already imaging yourself joining our team? Good, because we can’t wait to hear from you. Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and hope its yours If you’re curious to know more then we welcome your application no later than Where can I find out more? Our Social Media, Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/ Follow AstraZeneca on Facebook https://www.facebook.com/astrazenecacareers/ Follow AstraZeneca on Instagram https://www.instagram.com/astrazeneca_careers/?hl=en Show more Show less

Job Title: Senior Consultant - DevOps GCL: D3 Introduction to role At AstraZeneca, we treat Scientific Computing as a strategic asset that underpins our advances in science. Leading-edge research strategies critically depend on elite computing capabilities and high-energy engineering teams supporting them. The Scientific Computing Platform (SCP) is AstraZeneca's innovative computing environment designed to tackle today's and tomorrow's in-silico challenges. It focuses on a platform concept, building capabilities and services around central building blocks. At its heart, it uses compute environments, a classical InfiniBand/Slurm HPC cluster, an Openstack private cloud, and various public clouds for elasticity and scale. To exploit these resource pools most efficiently, the SCP deploys strong DevOps tooling and cloud-native technologies, aiming to adjust and adapt according to changing requirements and follow the science. The engineers and architects in the SCP team are key to continuously delivering and supporting this critical capability. Accountabilities We are looking for a highly motivated, ambitious, and independently working Scientific Computing engineer to join our global team. If you combine a DevOps way of working with a strong enterprise-ready service attitude, problem-solving skills, excitement for technology, and interest in accelerating science, then you are in good company. You will be engaged in a variety of activities stretching from daily operations and development, exciting technology exploration, and strategic project delivery. You will own parts of the platform, drive its operational excellence, prioritize the development backlog, and craft the roadmap. Whether your interest is more operations or development-focused, classical HPC or cloud computing, in hardware or applications, our team operates the whole stack. Everyone on the team takes responsibility for our success. Based in one of the science hub sites, you will become a trusted partner to our Science community, ensuring that we deliver technology at the highest standards to enable and push their work to the next level. Translating their needs into efficient solutions and applying engineering excellence to make science successful will be your daily reward. We operate the SCP as a single global team with shared responsibilities. You will join an agile and hardworking team of technologists who share excitement for High-Performance & Big Compute, modern technology stacks, and their application in science to change the lives of patients. To us, teammates are people who have humility, feel accountable for their work (and their teams), as well as the ability and willingness to be a leader of something. Living and breathing technology is a key factor enabling us to keep pace with the life-changing ideas of AstraZeneca's scientists. Essential Skills/Experience Demonstrated expertise and 10+ years of hands-on experience operating, crafting, or engineering large-scale computing environments, with a main focus on High-Performance Computing (HPC) while having experience in DevOps practices. Demonstrable ability to drive innovative computational solutions and leverage emerging technologies within the Life Sciences domain, particularly in the Pharmaceutical Industry or Biotech sectors. Nice to have experience in administering large-scale cluster and server computing environments, utilizing related software such as Slurm, LSF, and Grid Engine. Hands-on experience collaborating within DevOps teams and applying agile methodologies to streamline operations and development processes. Providing comprehensive scientific software support for end-users, including configuration, installation, tuning, and maintenance. Proficiency in operating and managing virtualized private cloud resources, specifically with OpenStack. Solid understanding of Linux system administration, the TCP/IP stack, and storage subsystems. Knowledge in administering large-scale parallel filesystems, including GPFS and Lustre. Proven track record of using configuration management tools (e.g., Ansible, Salt, Puppet) and technology frameworks within IT operations. Experience in developing and managing relationships with third-party suppliers. Proficient in scripting and tool development for HPC and DevOps platforms using Bash and Python. Desirable Skills/Experience Familiarity with operating and configuring public cloud computing infrastructure, such as AWS, Azure, or GCP. Experience in managing virtualized private cloud environments, particularly with OpenStack. Knowledge of container technologies (e.g., LXD, Singularity, Docker, Kubernetes). Demonstrated development experience across multiple programming languages, tools, and technologies (e.g., Java, C++, Python, Ruby, Perl, SQL, AWS). Familiarity with HashiCorp tools like Terraform, Vault, Consul, and Nomad. Experience in platform engineering, software engineering, and machine learning best practices, including version control, continuous integration (CI), continuous development (CD), containerization, and shell scripting. Bachelor's degree required; emphasis on Computational, Physical, or Biological Science, Engineering, or related fields preferred. A Master's or Ph.D. is a plus. Solid understanding of analytic products and scientific computing software relevant to pharmaceutical R&D. Excellent written and verbal communication, teamwork, and collaboration skills. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, our work has a direct impact on patients by transforming our ability to develop life-changing medicines. We empower the business to perform at its peak by combining cutting-edge science with leading digital technology platforms and data. Join us at a crucial stage of our journey in becoming a digital and data-led enterprise. Make the impossible possible by building partnerships and ecosystems while driving scale and speed to deliver exponential growth. Here you'll find countless opportunities to learn and grow while working on innovative technologies. Ready to make a difference? Apply now! Show more Show less

About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. Typical Accountabilities: As a regional technical expert develops and maintains or project manages the study management process and technology required in clinical trials Acts as a source of knowledge in area of expertise, defining and communicating important initiatives across departments and functions As a project manager plans and leads the delivery of all components of a clinical study to time, quality, budget, project standards, company quality standards, and scientific requirements from the study design team As a project manager leads preparation and delivery of study documents As an expert accountable for specialised research or delivery of internal reports to enhance the effectiveness of study management contributions to worldwide submissions across a range of products Applies expert statistical skills to support internal proposal development and external regulatory submissions Keeps own knowledge of best practices and new relevant developments up to date Leads and implements globally agreed study delivery and Clinical Development strategies including process and technology related to Study Delivery Typical People Management Responsibility (direct / indirect reports): Approximate number of people managed in total (all levels) - 10 Matrix Manager – (projects/dotted line) What is the global remit? (how many countries will the role operate in?): Own country Education, Qualifications, Skills and Experience: Essential: Bachelor’s degree in relevant discipline; Significant experience in Study Management within a pharmaceutical or clinical background; Thorough knowledge of Patient Safety processes and local regulations Desirable: Advanced degree within field; Professional certification; Clinical study delivery operational experience; Project management experience Key Relationship to reach solutions: Internal (to AZ or team): Study Management function; Development function; Other AstraZeneca employees External (to AZ): External service providers and regulatory bodies Why AstraZeneca? At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. Show more Show less

Job Title: Documentation Specialist- Clinical Pharmacology & Safety Science Introduction to role: Are you ready to dive into the world of clinical pharmacology and safety science? As a Documentation Specialist, you'll play a pivotal role in supporting regulatory submissions and reports within the Clinical Pharmacology and Quantitative Pharmacology (CPQP) department. Your expertise will guide project teams through the technical requirements of clinical submissions, ensuring compliance and excellence throughout the product lifecycle. You'll be at the forefront of building clinical regulatory documents and submissions, handling compliance in the AZ Regulatory Document Management system (ERV), and providing functional training and support. Are you prepared to make a difference? Accountabilities: With general supervision, you'll chip in to the preparation and compilation of regulatory submissions, ensuring timeliness and quality within the following areas: Generate quality and clinical basic structures and content for regulatory submissions and documents. Apply relevant regulatory-authority compliant document naming conventions. Import and create documents for regulatory submissions, including referenced literature and reference lists. Edit submission documents, including cross-referencing citations, creating abbreviations lists, and formatting data tables. Ensure submission readiness conformance with house-style, AstraZeneca’s submission ready standards, and regulatory agency requirements. Format Word documents, perform PDF editing, and ensure navigable submission documents. Give to the preparation and maintenance of submission document templates. Participate in project teams related to deliverables standards or harmonization within the team scope. Administer and provide end-user support for tools used within Biopharmaceutical Development, including ERV Document Management System. Essential Skills/Experience: Bachelor’s degree or equivalent industry-relevant experience Awareness of basic principles of GXP and ICH (International Conference on Harmonization) Basic understanding of CTD (Common Technical Document) content and formatting standards Proficiency in Microsoft Office Experience working within validated electronic document management systems Familiarity with working within SharePoint Basic knowledge of information management and document management tools Proficient in the English language Excellent written and verbal skills (English) Desirable Skills/Experience: 1-2 years of industry experience in validated electronic document management systems Knowledge of the basic principles of the drug development process Basic understanding of principles of CFR21 part 11 requirements and other global standards Experience with Adobe Acrobat and related ISI tools (e.g., ISI toolbox) Experience as SharePoint site owner Good social skills and ability to establish relationships Strong communication skills with all levels of the organization Ability to deal with ambiguity and changing priorities Good attention to detail Able to follow written standards, procedures, and processes When we put unexpected teams in the same room, we ignite bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, we are driven by curiosity and courage, exploring new scientific frontiers to tackle some of the world's most complex diseases. Our commitment to innovation is motivated by a passion for science, empowering us to make bold decisions without fear of failure. We collaborate seamlessly across diverse teams, leveraging global knowledge to create impactful solutions. With opportunities for lifelong learning and career growth, AstraZeneca is where you can truly make a difference in patients' lives. Ready to embark on this exciting journey? Apply now to join our team! Show more Show less

Job Title: Director- Data, Analytics & AI, Cheminformatics GCL- F Introduction to role AstraZeneca has invested heavily in our Augmented Drug Design-Make-Test and Analyse platforms as we seek to deliver better, differentiated candidate drugs into trials faster, for greater patient benefit. We have made great strides in creating an ecosystem enabling operational and experimental data capture, and in developing AI/ML analytics, AI, and ML services for both traditional small molecules and complex modalities that will pave the way for this transformation. The next stage of this journey involves building a unified scientific data and AI platform with state-of-the-art algorithms and technology that will enable our scientists to design new and safer drugs faster. We are looking for a Lead Cheminformatics Engineer who can excel in both cheminformatics and software development to join our team to help build and modernize our integrated software platform supporting key drug discovery science. In Early Science, we have highly skilled scientists generating ideas and performing experiments supporting complex drug discovery projects. Our environment is driven by scientific and technical innovation with a high degree of diversity in workflows, data, vendor solutions, and in-house builds. Working alongside Computational and Medicinal Chemists, Software and Data Engineers, Architects, and Analysts, you will lead in designing and implementing scientific solutions end-to-end. You will use your scientific knowledge and technical acuity to troubleshoot and provide innovative solutions to ensure smooth experiences for our scientists as well as for the software development team. Your work will have a direct impact on the science we do, and you have an opportunity to enable our scientists to undertake science that is not possible today. Accountabilities You will join a global team of cheminformaticians, scientific software engineers, and devops engineers in our Augmented-DMTA platform and perform the following: Be one of the subject matter experts for the team with knowledge of cheminformatics and computational chemistry tools used in drug discovery Work with cutting edge technology stack in a cloud environment solving scientific challenges for drug discovery Be responsible for designing and implementing scientific software and data solutions to make our science easier to do, easier to learn from, and offer faster delivery and higher quality across all therapeutic areas Design and build novel products and features to address long-standing problems in drug discovery with a focus on producing amazing user experiences that are more than the sum of their parts Collaborate with product, design, data science, software engineering, and scientists to build cutting-edge experiences and services Propose and implement changes to our drug discovery data models, core architecture, and codebase Develop all levels of the technical stack even if you’re more experienced in some layers with a strong focus on scalable backend services Support less experienced software engineers by knowledge sharing, mentoring, and feedback Proactively review and improve the scalability, reliability, performance, and availability of drug discovery services Advocate for rigorous engineering practices and discipline: code reviews, automated testing, logging, monitoring, alerting, etc. Be passionate for staying on top of tech trends, experiment with and learn new technologies, participate in internal & external technology communities, and mentor other members of the engineering community Propose solutions for engineering problems deploying critical thinking and analysis skills Essential Skills/Experience Expertise in Cheminformatics, ML, or a related field and experience working with one of the cheminformatics toolkits Expertise in one or more languages like Python, Java, Node.js with the willingness and ability to quickly adapt to a new language Some experience with end-to-end web development with at least one of the web frameworks, FastAPI, Flask, Spring, Django, etc. Experience working with relational and/or NoSQL databases and knowledge of query optimization techniques Proficiency in Linux environments Demonstrable abilities with the coding best practices including testing, code review, and version control Excellent teamworking, verbal, and written communication skills Desirable Skills/Experience CI/CD experience with some automation tooling like Jenkins, TravisCI, Github actions, etc. Demonstrable high proficiency in data structures and design patterns Experience in chemistry data standardization, transformation and harmonization combining multiple data sources Experience in cloud services and tools Experience data and/or compute pipelining tools either generic or cheminformatics-specific ones Basic understanding of Machine Learning concepts and MLOps Experience with Docker and Kubernetes Experience with GitOps When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, our work has a direct impact on patients by transforming our ability to develop life-changing medicines. We empower the business to perform at its peak by combining cutting-edge science with leading digital technology platforms and data. Join us at a crucial stage of our journey in becoming a digital and data-led enterprise. Here you can innovate, take ownership, explore new solutions with leading-edge technology, and tackle challenges that might never have been addressed before. Our dynamic environment offers countless opportunities to learn and grow while making meaningful contributions. Ready to make an impact? 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Job Title: Regulatory Affairs Manager II (Packaging & Artwork) Career Level: D Introduction to role: Are you ready to lead the charge in transforming drug development strategies into reality? As a Regulatory Affairs Manager II, you'll be at the forefront of coordinating, developing, and implementing new and revised printed labeling for our commercial products. Your expertise will ensure that packaging components meet regulatory standards across the US, export markets, and EU centralized procedures. Dive into a role where your strategic input and leadership in cross-functional activities will drive continuous improvement in processes and tools. Accountabilities: What you'll do: Ensure all work is performed in accordance with established procedures, regulatory requirements, and GxPs. Serve as the point of contact for managing all labeling/artwork requests for allocated products requiring market/regulatory approval in the US, markets receiving a standard export pack, and EU centralized procedures. Coordinate and/or lead the development and lifetime maintenance of packaging component labeling for commercial products, including new pack introductions, product launches, updates to existing packs, and mock-ups for regulatory submissions. Collaborate with marketing company colleagues regarding global artworks as appropriate. Engage with operations/manufacturing sites regarding implementation of global artworks as needed. Ensure proper version control and document integrity of packaging component labeling, printed labeling artworks, and other assigned labeling documents. Process and prepare all final printed labeling for the US and required EU specimens for submission. Essential Skills/Experience: Relevant university degree in science or related discipline Minimum 7 years of regulatory experience within the biopharmaceutical industry, preferably working with labeling Keen attention to detail and accuracy Thorough knowledge of labeling regulations and guidance Strong project management skills Leadership skills, including experience leading multi-disciplinary project teams Desirable Skills/Experience: Experience in packaging labeling development and/or maintenance Experience working with stakeholders from locations outside of India, especially Europe and/or USA When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, innovation drives us forward. We are committed to pushing beyond traditional regulatory approaches to develop progressive solutions that prevent and treat diseases. Our diverse team thrives on curiosity and collaboration, empowering us to make quick decisions and influence drug development strategies. With a focus on technology adoption and automation, we strive for efficiencies that bring life-changing medicines to patients faster. Here, you'll find a supportive environment where your professional growth is nurtured through our Regulatory academy and development path. Ready to make an impact? Apply now to join our dynamic team and be part of shaping the future of medicine! Show more Show less

Job Title:Assistant Manager – Data Stewardship/Manager – Data Stewardship Career Level : D3 Introduction to role Are you ready to take charge of data quality and drive impactful change? As an Assistant Manager - Data Steward, you will be responsible for ensuring the integrity and accuracy of data within CRM and MDM systems. Your role will involve routine reporting, managing data change requests, standardizing data, conducting research, cleansing, de-duplication, and enforcing quality standards and best practices. Join us in shaping the future of data stewardship! Accountabilities The Data Steward will manually update attributes of managed records to enhance core data, getting in touch with users for verification and updating provider affiliation information via Data Change Requests. You will manage customer data change requests, ensuring timeliness and adherence to standard operating procedures. Your role includes applying business and compliance rules, performing ad-hoc data analysis and extracts, and ensuring new data elements are accurately applied without duplication. You will audit the data quality of peers, coordinate tasks with IT teams, maintain alignment between CRM and MDM systems, process GDPR-related requests, and validate client information. Additionally, you will implement process transitions and stabilization, develop data quality processes, and automate recurring tasks. Essential Skills/Experience Strong analytical and problem-solving skills People management experience Strong knowledge on databases and database concepts, SQL, analytical tools Familiarity with MS Office Tools – Word, Excel, PowerPoint Document processes and adhere to standard operating procedures and processes Basic project management skills and be detail oriented Capable of managing multiple projects/requests simultaneously Work in teams, Collaborate and ensure Compliance Basic to limited exposure to issue/ticket management and/or tracking tools (ex: JIRA, ServiceNow) Desirable Skills/Experience Exposure to MDM tools and systems – Reltio, Veeva Good experience in Process transitions, Building teams & Process Maturity model Familiarity with tools like PowerBI, Snowflake, Python Industry Data knowledge – OneKey, Veeva Open Data, Definitive Health Care data, Payer Data etc. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, you'll be part of a distributed team that drives excellence and breakthroughs. Here, your skills can genuinely impact patients' lives. We're on an exciting journey of growth through innovation, reimagining how we work by harnessing radical technologies. Every person plays a vital role in our story—take initiative, challenge norms, and make quick decisions. With a strong network for sharing and learning, you'll be surrounded by high performers who inspire you to learn more. We focus on finding better ways to partner with the business and help AstraZeneca achieve its ambitions. Ready to make a difference? Apply now and be part of our dynamic team! Show more Show less

About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. Job Description To create and track the conference calendar for Oncology Business Unit. Work with Medical Team, Marketing team and Zonal Business Manager to understand the scientific needs in the region. Engage with HCPs to understand the platforms for scientific dissemination and to align with scientific needs/capability of AZ. Ability to negotiate with stakeholders to provide an adequate and appropriate representation for AZ on major scientific platforms Ensure compliance with the AZ Code of Ethics, Global External Interactions Policy and Standards, and Privacy Policy and Standards, especially when interacting with HCPs/Third Party. Coordinate and execute end-to-end function for conference partnership with HCO. Eligibility: University Science graduate., Bachelors degree 3+ years of sales/marketing experience required. Experience In Super- Speciality / Oncology Preferred. Aptitude for establishing and nurturing strategic relationships. Comprehensive understanding of the Pharmaceutical Industry. Effective Influencing and Communication Skills. Proficiency in Customer Management. Strong Commercial Acumen. Organizational skills, good analytical skills / mind stability to manage complexity with a high degree of maturity. Why AstraZeneca? At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. Show more Show less

About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. Job Description To create and track the conference calendar for Oncology Business Unit. Work with Medical Team, Marketing team and Zonal Business Manager to understand the scientific needs in the region. Engage with HCPs to understand the platforms for scientific dissemination and to align with scientific needs/capability of AZ. Ability to negotiate with stakeholders to provide an adequate and appropriate representation for AZ on major scientific platforms Ensure compliance with the AZ Code of Ethics, Global External Interactions Policy and Standards, and Privacy Policy and Standards, especially when interacting with HCPs/Third Party. Coordinate and execute end-to-end function for conference partnership with HCO. Eligibility: University Science graduate., Bachelors degree 3+ years of sales/marketing experience required. Experience In Super- Speciality / Oncology Preferred. Aptitude for establishing and nurturing strategic relationships. Comprehensive understanding of the Pharmaceutical Industry. Effective Influencing and Communication Skills. Proficiency in Customer Management. Strong Commercial Acumen. Organizational skills, good analytical skills / mind stability to manage complexity with a high degree of maturity. Why AstraZeneca? At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. Show more Show less

Job Title: Associate Director Information Management & Digital Solutions Career level: E Introduction to role: Do you want to play a key role in the digital transformation within a Global Engineering organization? We are looking for a visionary and driven Associate Director Information Management & Digital Solutions to accelerate our digital journey, with a strong focus on data management, digital solutions, and artificial intelligence (AI). Our Global Engineering (GE) team is at the forefront of innovation, establishing cutting-edge facilities worldwide where AstraZeneca advances science to deliver life-changing medicines. We scope, plan, and implement major capital projects across our Operations sites, ensuring maximum business lifecycle benefits. We also provide strategic advice, helping the business make informed asset decisions while integrating the latest technology. Are you ready to make a real impact in an organization where technology and sustainability go hand in hand? Then we want to hear from you! Accountabilities: As the Information Management Digital Solutions Lead, you'll oversee the development and execution of our information management strategy, ensuring that information assets support wider business objectives. Your ability to identify opportunities, create structure, and turn strategy into tangible value will be essential. Your role will be pivotal in making information easily accessible and appropriately stored, enabling data-driven decisions that propel us forward. Other responsibilities include: Lead, mentor, and develop a team of Information management specialists. Provide framework, standards, and guidelines to ensure optimal Information Management in GE and GE-led projects Identify, implement, and train colleagues on data management best practices and use of tools and templates Act as Data Product Manager (DPM), owning GE Data products and representing GE in Global Operations and IT Data Product Manager networks Lead data, master data, and information governance processes to ensure compliance and high standards of data/information quality within GE (and AZ) Act as workstream lead for Digital, Data, and AI-related initiatives as part of GE overall Strategy Manage GE’s digital platforms to ensure they are accurate and align with AZ standards Develop, maintain, and improve digital solutions that use existing tools (e.g., SharePoint, PowerBI) to optimize data management and enhance reporting Identify/evaluate opportunities to develop digital solutions that use existing tools to streamline data collection, reporting, and optimize GE’s processes Collaborate with Process owners to identify and devise solutions that optimize business process performance and capability Work with business users to understand solution needs and requirements Troubleshoot issues with the current application as well as participate in the development of new product features Ensure and monitor compliance by team members and third parties by positively reinforcing the Code of Conduct and all relevant AstraZeneca Policies and Standards Essential Skills/Experience: BA / BS computer science/information technology or life sciences degree 5+ years experience in the development, design, storage, and distribution of information management tools, publications, and forms Operations programming experience is required Proficient computer skills across multiple applications 5+ years experience managing teams Desirable Skills/Experience: Custom Solutions development experience is preferred Understanding of Lean principles and methodologies When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, you'll find yourself in an inclusive network of diverse teams where support, trust, and respect are paramount. Our commitment to delivering accelerated growth drives us to keep building on our foundations as we turn our complex pipeline from molecule to medicine. With innovative science, digitalization, and sustainable practices at the heart of what we do, you'll be part of a community that supports each other on their journeys. Experience a sense of belonging like no other as you contribute to making people's lives better. Ready to step up and lead? Apply now to join us on this exciting journey! Show more Show less