409 Statistical Programming Jobs

Role Overview: You will provide expertise under the Global Head, Statistical Programming in AQS Development, focusing on quality, CDISC standards, open-source capabilities, automation, and data structures for modeling. This role requires extensive experience in drug development, GCP, and regulatory requirements. You will enhance open-source programming capabilities and programming/reporting standards across therapeutic areas, acting as an influential leader representing Statistical Programming at leadership meetings, overseeing and coordinating all functional activities, and collaborating to ensure consistency in programming practices across sub-functions. Your initiatives will lead to estab...

Synopsis of the role Join our Identity and Fraud Solution Analytics group as a Data Scientist, where you will play a pivotal role Analyze multiple complex data sources using statistical analysis and programming languages to inform business decision making. Delivers analytical and commercial solutions for internal and external customers. Develops models and other analyses to test hypotheses and understand the potential impacts of decisions under various scenarios. Able to communicate analytical results to generate improved business decisions and profitability. Combines business requirements and existing processes and data knowledge to create analytical solutions. What You'll Do Utilize combin...

About The Job Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main Responsibilities The Principal Biostatistician will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans (SAP), programming specifications for a...

Role Overview: As a Manager in the Solutions Design team at Delhivery's end-to-end supply chain division, you will play a crucial role in understanding complex logistical challenges faced by potential customers across various segments. Your primary responsibilities will include conducting data analysis, number crunching, and providing data-backed supply chain solutions encompassing WH Footprint, Network Design, Vehicle Selection, Warehousing, and Omnichannel distribution. Additionally, you will be tasked with identifying avenues to enhance profitability for existing accounts. Key Responsibilities: - Drive analytics projects related to supply chain solutions, Network design, and Warehousing D...

Statistical Programming review of Case Report Forms (CRFs), annotated CRFs, database structures and study related documentation (e.g. data validation guidelines),Develop SAS programs for ad hoc tables and listings, Required Candidate profile Design and set-up utilities/SAS based systems ,Carry out electronic data transfer (both incoming and outgoing),Review and interpret Report and Analysis Plans, Follow CDISC, FDA & other Guidelines

Key Responsibilities Project Responsibilities: Provides comprehensive programming leadership and support to clinical project teams and vendors, including deployment of programming strategies, standards, specifications and programmed analysis to comply with regulatory requirements, SOPs and work practices Independently develops, validates, troubleshoots, and maintains complex programs and utilities in accordance with predefined specifications and standards Leads / Supports the electronic submission preparation and review Develops unambiguous and robust programming specifications (e.g. ADaM specifications) Reviews key planning documents (e.g., statistical analysis plan, data presentation plan,...

Career Category Research Job Description Associate Director, Biostatistical Programming HOW MIGHT YOU DEFY IMAGINATION If you feel like you re part of something bigger, it s because you are. At Amgen, our shared mission to serve patients drives all that we do. It is key to our becoming one of the world s leading biotechnology companies. We are global collaborators who achieve together researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It s time for a career you can be proud of. Join us. Associate Director, Biostatistical Programming What you will do Let s do this. Let s change the world. Amgen is expanding its Global Statistical Pro...

ISS - Statistical Programmer II - India ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Statistical Programmer II to join our diverse and dynamic team. As a Statistical Programmer II at ICON, you will play a vital role in the development, validation, and execution of statistical programs to support clinical trial analysis and reporting. Your expertise will contribute to the accurate interpretation of clinical data, helping to ensure the successful delivery o...

Senior Manager Credit Risk Location Gurgaon / Bangalore / Mumbai PayU, the fintech-arm of Naspers, is a leading financial services provider in global growth markets. We use our expertise and heritage in cross border and local payments to extend the services we offer to merchants and consumers. Our innovative technology, developed in-house as well as through investments and strategic partnerships, empowers billions of people and millions of merchants to buy and sell online, extending the reach of financial services. PayU specialises in credit products and services for emerging markets across the globe. We are dedicated to removing risks to merchants, allowing consumers to use credit in ways t...

Career Category Research Job Description Senior Manager, Biostatistical Programming HOW MIGHT YOU DEFY IMAGINATION If you feel like you re part of something bigger, it s because you are. At Amgen, our shared mission to serve patients drives all that we do. It is key to our becoming one of the world s leading biotechnology companies. We are global collaborators who achieve together researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It s time for a career you can be proud of. Join us. Senior Manager, Biostatistical Programming What you will do Let s do this. Let s change the world. Amgen is expanding its Global Statistical Programming...

Job Summary This job will develop and implement data science models and algorithms to support business needs. You will work with stakeholders to understand data requirements and deliver solutions. Your role involves ensuring data quality, optimizing data processes, and collaborating with cross-functional teams. Job Description Essential Responsibilities Develop and implement data science models and algorithms. Analyze and interpret complex data sets. Ensure data quality and integrity. Collaborate with stakeholders to understand data requirements. Optimize data processes for efficiency and performance. Perform advanced statistical analysis and reporting. Expected Qualifications Minimum of 2 y...

An Individual Contributor role Productive hands on programming, supporting deliverables in the study / project / portfolio / standards team, of medium high complex statistical programming deliverables to support assets and study teams Performs tasks with limited supervision early in role and independently later in role. Is capable of handling standards/study programming specific activities independently including collaboration across stakeholders at various timezones Ensures adherence to high quality programming standards in their daily work Ensure the tasks are completed on time with quality and are compliant to the process at Pfizer with needed guidance. Work collaboratively with study tea...

An Individual Contributor role Productive hands on programming, supporting deliverables in the study / project / portfolio / standards team, of medium high complex statistical programming deliverables to support assets and study teams Performs tasks with limited supervision early in role and independently later in role. Is capable of handling standards/study programming specific activities independently including collaboration across stakeholders at various timezones Ensures adherence to high quality programming standards in their daily work Ensure the tasks are completed on time with quality and are compliant to the process at Pfizer with needed guidance. Work collaboratively with study tea...

PRINCIPAL STATISTICAL PROGRAMMER (12 15 YEARS) LOCATION: ANYWHERE IN INDIA WORK MODE : Hybrid ROLES and RESPONSIBILITIES: Implementation of statistical programming strategy related to innovation in technologies, automation, processes, and standards to maximize efficiency Support the development and implementation of a programming ecosystem to enable successful project deliverables Review statistical analysis plans, mock-shells, database set-up specifications Validate or Review the Programming packages (includes the aCRFs, specifications and datasets, Define.XML and Reviewer's Guides (for both SDTM and ADaM) Develop department programming standards to meet business needs and regulatory requir...

About the Company Qinecsa is a trusted, global partners bringing together best-in-class technology and scientific expertise to connect life science companies, public health, and regulatory sectors to the right safety solutions. we take pride in being the leading specialist pharmacovigilance provider, offering unparalleled expertise in PV services, technology, and consulting to cater to the unique needs of small, medium, and large pharmaceutical companies. About the Role We are seeking a Director of Technical Engineering to lead the technical design and development of pharmacovigilance signal detection solutions based on our flagship Qinecsa Vigilance Workbench signal detection platform. The ...

At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing. Our therapeutic expertise spans renal, cardiometabolic, and oncologyareas where we make a significant impact on improving global health. At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring div...

Responsibilities : Key Responsibilities Work on end-to-end data science engagements from problem definition to solution development. Design and implement advanced analytical models and process frameworks. Collaborate with different stakeholders, providing domain and technical thought. Perform Fit/Gap analysis and translate business needs into actionable data solutions. Ensure compliance with release governance and manage incidents using industry-standard tools. Contribute to Unit/Organizational initiatives, including Centers of Excellence (COEs). ________________________________________ Additional Responsibilities: . Technical and Professional Requirements: Required Skills & Experience 4+ ye...

Carrying out preprocessing of structured and unstructured data Enhancing data collection procedures to include all relevant information for developing analytic systems Processing, cleansing, and validating the integrity of data to be used for analysis. Analyzing large amounts of information to find patterns and solutions. Developing prediction systems and machine learning algorithms Presenting results in a clear manner Propose solutions and strategies to tackle business challenges. Data mining or extracting usable data from valuable data sources. Using machine learning tools to select features, create and optimize classifiers Requirements Programming Skills knowledge of statistical programmi...

As a Statistical Programmer at ProPharma, your role involves providing statistical programming and validation for life sciences-related projects, including clinical trial datasets and tables, listings, and figures. You will access and convert data to SAS datasets and other file types from database management systems and PC file formats. Collaborating with external vendors to develop and monitor the content and structure of SAS datasets and other files is also part of your responsibilities. Working closely with statisticians and other statistical programmers, you will generate and validate outputs to ensure accuracy and the quality of statistical programming algorithms. Additionally, you will...

As a Statistical Programmer I, you will be responsible for creating, testing, and maintaining programs for clinical studies using SAS. Your key responsibilities will include: - Using SAS to generate summary tables, data listings, graphs and derived datasets as per statistical analysis plan and programming specifications. - Ensuring that outputs meet quality standards and project requirements. - Performing validation programming and collaborating with team members to resolve discrepancies. - Keeping project team members informed of programming progress and issues. - Following SOPs and relevant regulatory guidelines. - Maintaining well-organized project documentation and verification/quality c...

Company Description Oryxion is at the forefront as a full-spectrum Data CRO, providing services across Clinical Data Management, Data Visualization, Statistical Programming, Biostatistics, Medical Writing, and Regulatory Affairs. We integrate AI-enabled analytics to ensure accurate and streamlined data flow, from initial patient engagement to final submission. Our advanced ecosystem incorporates EDC, ePRO, IWRS, eTMF, and CTMS tools for efficient data management. With expertise in complex trial designs and various therapeutic areas, our team has contributed to over 700+ Global Regulatory Submissions and has significant End-to-End Clinical Development experience. Role Description This is a fu...

Roles and Responsibility Design, develop, and implement clinical SAS programs for data management and analysis. Collaborate with cross-functional teams to identify business requirements and develop solutions. Develop and maintain complex SQL queries for data extraction and manipulation. Troubleshoot issues related to clinical SAS programs and provide technical support. Participate in code reviews and ensure adherence to coding standards. Stay updated with industry trends and emerging technologies in clinical SAS and SQL programming. Job Requirements Strong knowledge of clinical SAS programming language and its applications in data management and analysis. Expertise in SQL programming for dat...

Roles and Responsibility Design, develop, and implement clinical trial data management systems using SAS. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and maintain complex statistical analysis plans and programs. Troubleshoot and resolve technical issues related to clinical trial data management. Ensure compliance with regulatory requirements and company standards. Participate in project planning, execution, and reporting activities. Job Requirements Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience working with large datasets and developing complex statistical analysis plans. ...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Collaborate with cross-functional teams to ensure timely and accurate data delivery. Conduct statistical review of case report forms, annotated CRFs, database structures, and study-related documentation. Provide statistical input into protocol development and review. Ensure compliance with regulatory requirements and company policies. Mentor junior statisticians and provide guidance on statistical methodologies. Job Requirements Strong knowledge of statistical concepts, including regression, time series, mixed effects, and predictive modeling. Experience with statistical software packages such as S...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Provide statistical input into protocol development and review. Ensure compliance with regulatory requirements and company policies. Mentor junior statisticians and provide guidance on statistical methodologies. Job Requirements Strong knowledge of statistical concepts, including regression, time series, mixed effects, and survival analysis. Experience with statistical software packages such...