127 Protocol Development Jobs

As a Clinical Development Manager at Azurity Pharmaceuticals, you will play a crucial role in supporting departmental activities related to clinical trials and scientific analyses across therapeutic areas. Reporting to the Associate Director, Clinical Development, you will have the opportunity to contribute to the success of the organization by leveraging your expertise and skills. Your responsibilities will include but are not limited to: - Ability to understand integrated data from clinical trials and other sources to provide scientific evaluations and develop risk assessments. - Providing operational and scientific oversight of nonclinical and clinical studies, ensuring compliance with GC...

Role & responsibilities Develop and customize IEC 60870-5-104 protocol stack in C/C++ with additional data structures, frames, and security layers. Implement and secure masterslave communication for SCADA servers, RTUs, NMS, and NAS systems . Work on TCP/IP protocols, socket programming, and server implementation across Windows & Linux platforms . Apply IEC standards (IEC 62351, cybersecurity protocols) for secure communication and system compliance. Perform network/server troubleshooting, optimization, and documentation for critical power automation systems. Preferred candidate profile Bachelors / Masters in Electrical, Electronics, Computer Science, or related engineering . 3–7 years of ex...

Debugging and Troubleshooting: Utilize debugging tools (e.g., oscilloscopes, logic analyzers, hardware debuggers) to diagnose and resolve software and hardware issues. Networking Expertise: Development exp on Layer2 and Layer3 protocols like MPLS,BGP,OSPF,VLAN,IPV Hardware Integration: Collaborate with hardware engineers to integrate software with hardware components, ensuring seamless functionality. Software Development: Design, implement, and test embedded software solutions using C/C++ for network-enabled devices. Debugging and Troubleshooting: Utilize debugging tools (e.g., oscilloscopes, logic analyzers, hardware debuggers) to diagnose and resolve software and hardware issues. Networkin...

Meet the Team The Catalyst Engineering IOS XE Platform Independent team at Cisco builds and develops high-performance system software for a range of Cisco platforms, including enterprise switches and routers, as well as service provider routing platforms. As industry leaders driving innovation in the enterprise sector, the team operates at the forefront of a constantly evolving market. Joining this multifaceted group offers boundless opportunities to grow your career and contribute to ground-breaking advancements in networking technology. Your Impact We will develop and integrate products used by leading enterprises worldwide, working on the IOS XE OS that serves as the backbone of many ente...

About the job As a Principal Biostatistician, youll Lead or support one or several early/late phase studies, under minimum supervision of statistical team leader.We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve peoples lives. Were also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Main responsibilities : Support the clinical study design (including protocol development), the study setup and conduct. Conduct the statistical analyses according to the SAP, prepare statistical methods & provide statist...

Major Responsibilities : Support the clinical study design (including protocol development), the study setup and conduct. Conduct the statistical analyses according to the SAP, prepare statistical methods & provide statistical insight into interpretation and discussion of results sections for the clinical study report (CSR) and/or publications to ensure the statistical integrity of the content according to internal standards and regulatory guidelines and in compliance with SOPs. Accountable for all assigned statistical deliverables related to one study or specific domain: statistical sections in protocol including sample size calculation, randomization specifications, and statistical methodo...

Role Overview: As the Clinical Data Manager, you will be responsible for overseeing all data management activities related to Phase I-IV clinical trials. Your role will involve ensuring compliance with ICH/Good Clinical Practices (GCP) and other relevant guidelines to maintain high-quality work products and meet timelines and deliverables. Key Responsibilities: - Participate as the primary data management representative on the QED multidisciplinary project teams. - Serve as the main point of contact for all data management interactions with the Sponsor. - Contribute to protocol developments and reviews, as well as review of clinical study reports and statistical analysis plans. - Assist in t...

As a highly experienced and self-driven Systematic Literature Review (SLR) freelancer in the life sciences domain, you will be responsible for supporting end-to-end SLR development and strategic insight generation. Your proven track record in designing and executing high-quality SLRs, rapid reviews, and literature-based deliverables aligned with GPP, PRISMA, and other industry standards will be essential for this role. Key Responsibilities: - Lead the full lifecycle of SLR projects from protocol development to screening, data extraction, analysis, reporting, and publication support. - Critically appraise ongoing work, identify potential quality issues or gaps before client delivery. - Develo...

You will be responsible for developing and adhering to comprehensive clinical trial protocols in collaboration with the Principal Investigator. Your key responsibilities will include: - Implementing effective strategies to recruit and retain study participants - Overseeing accurate and timely data collection entry and management - Ensuring all trial activities comply with regulatory guidelines and maintaining thorough documentation - Managing the clinical trial budget effectively, ensuring cost efficiency - Coordinating with cross-functional teams and providing necessary training to staff involved in the trial - Monitoring participant safety and managing adverse events promptly - Implementin...

Role Overview: Continental Hospital in Gachibowli, Hyderabad is looking for a Senior Clinical Pharmacologist to join their Clinical Pharmacy Services/Pharmacy & Therapeutics department. As a Clinical Pharmacologist with a minimum of 8 years of experience in a multispecialty hospital setting, you will be responsible for ensuring safe and effective medication use, collaborating with the medical team, and supporting patient care through your clinical expertise. Key Responsibilities: - Implement and monitor medication safety protocols to enhance patient safety and reduce errors. - Conduct thorough medication reconciliation during patient admission, transfer, and discharge to prevent discrepancie...

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. Provide statistical input into protocol development and review. Review and draft final production runs for projects to ensure quality and consistency. Mentor junior statisticians and provide training and guidance as needed. Collaborate with cross-functional teams to meet project deliverables. Job Requirements Strong knowledge of statistical concepts and techniques, including regression, time series, and mixed effects models. Experience with statistical software packages such as SA...

Estate Management -All estate operations including buildings, landscapes, and utilities. Maintenance Management Team & Contractor Management - external contractors/vendors and ensure work quality and timelines. Budgeting & Compliance

Roles and Responsibility Design, develop, and implement clinical trial protocols using SAS. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Develop and maintain complex statistical analysis plans and datasets. Troubleshoot and resolve technical issues related to clinical trial data management. Participate in project meetings and provide input on project scope and timelines. Ensure compliance with regulatory requirements and company standards. Job Requirements Strong knowledge of clinical trial design, protocol development, and statistical analysis. Proficiency in SAS programming language, including Base SAS and Enterprise Guide. Experience with...

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. Review and draft final production runs for projects to ensure accuracy and quality. 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 softwar...

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. Review and draft final production runs for projects to ensure accuracy and quality. 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 softwar...

Roles and Responsibility Design, develop, and implement clinical trial protocols using SAS. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Develop and maintain complex statistical analysis plans and datasets. Troubleshoot and resolve technical issues related to clinical trial data management. Participate in project meetings and provide input on project scope and timelines. Ensure compliance with regulatory requirements and company standards. Job Requirements Strong knowledge of clinical trial design, protocol development, and statistical analysis. Proficiency in SAS programming language, including Base SAS and Proc SQL. Experience with clinica...

Roles and Responsibility Collaborate with cross-functional teams to design and implement clinical research studies. Provide medical expertise and guidance on study protocols, informed consent forms, and case report forms. Develop and maintain relationships with investigators, site staff, and other stakeholders. Review and approve study-related documents, including protocols, informed consent forms, and case report forms. Ensure compliance with regulatory requirements and company policies. Participate in project team meetings and provide input on study progress and risks. Job Requirements Minimum experience in clinical research or a related field. Strong knowledge of clinical trial conduct, p...

About The Role Java Technical Manager/Architect | Hyderabad | 12 to 15 Years Leadership & Strategy Serve as the technical and strategic point of contact for two teams. Lead implementation strategies and own transformation initiatives across projects. Guide best practices and technical standards. Own and manage application support , ensuring reliability and efficiency. Stakeholder Engagement Act as a consultant to key stakeholders including enterprise architects, business leads, IT leads, and product owners. Provide strategic advice to stakeholders to support informed decision-making. Manage stakeholder relationships and align technical solutions with business goals. Collaboration & Coordinat...

About The Role - Grade Specific Tech Support Engineer Location :- Pune/Mumbai Experience :- 4 to 6 Years Choosing Capgemini Engineering means choosing a place where youll be empowered to shape your career, supported by a collaborative global community, and inspired to reimagine whats possible. Join us in helping leading organizations unlock the value of technology and drive scalable, sustainable growth. Your Role As a Tech Support Specialist, you will be responsible for providing technical assistance and support related to computer systems, hardware, and software. You will respond to queries, run diagnostic programs, isolate problems, and determine and implement solutions. In this role, you ...

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. Review and draft final production runs for projects to ensure accuracy and quality. 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 softwar...

We are looking for a Cyber Security & Ethical Hacking Specialist to safeguard systems, networks, and applications against evolving cyber threats. The ideal candidate will have hands-on expertise in Network Security, Certified Ethical Hacking (CEH), Web Application Penetration Testing (WAPT), and Bug Bounty Hunting. You will be responsible for identifying vulnerabilities, mitigating risks, and ensuring compliance with security standards to protect organizational assets. Roles and Responsibilities: Conduct penetration testing of web applications to identify vulnerabilities and weaknesses. Develop and implement effective threat detection and incident response strategies. Collaborate with develo...

As a Sponsor Coordinator at NHS Greater Glasgow and Clyde, you will have the exciting opportunity to join the Sponsor team of the largest R&I office in Scotland. This is a Fixed term post for 2 years, with the possibility of secondments. Your responsibilities will include coordination and delivery of an established portfolio of research, focusing on investigator-led non-CTIMP multicenter studies and drug trials involving multiple medicines at UK and international sites. Key Responsibilities: - Coordinate and deliver Sponsor activities for GG&C sole and Cosponsored trials with the University of Glasgow - Work closely with various teams including Project Management, Sponsor Research Pharmacy, ...

Role Overview: As the Principal Investigator (PI) based in Noida, India, you will oversee the scientific, ethical, and regulatory aspects of clinical trials. Your crucial responsibilities include ensuring participant safety, protocol adherence, and data integrity throughout the trial process. Collaboration with sponsors, regulatory authorities, and internal teams will be essential to achieve successful trial outcomes. Key Responsibilities: - Serve as the lead medical expert for assigned clinical trials - Ensure compliance with ICH-GCP guidelines and local regulatory requirements - Oversee patient recruitment and informed consent processes - Document and report adverse events - Participate in...

You will be working as an Asst Manager / Manager in the Biologics function of USV Private Limited in the Regulatory Affairs department specifically focusing on Clinical Trials for the EU and US markets. Your role will involve the following key responsibilities: - Developing Biosimilar Clinical Development Strategy, focusing on clinical trials and injectables for EU and US markets. - Designing and developing clinical protocols for Biosimilar Clinical trials, ensuring review and finalization for EU and US markets. - Handling Biosimilar Clinical Trial Applications, providing an overview of clinical study conduct, reviewing Clinical Study reports, and finalizing them for EU and US markets. - Aut...

Role Overview: The ideal candidate for the Biostatistician role should possess a Master's degree in Statistics or equivalent. A Ph.D. in Statistics or equivalent combined with 6 years of industry-related experience is also a preferred qualification. With at least 9+ years of experience, you must demonstrate a deep understanding of statistical and clinical trials methodology as it pertains to clinical development. As a Biostatistician, you will be an integral part of cross-functional development teams, contributing to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Your role will involve collaborating with various st...