- Amgen (Washington, DC)
- …team. Join us and transform the lives of patients while transforming your career. ** GCP Quality Compliance Manager** **What you will do** Let's do this! Let's ... for continuous improvement. + Provide hands-on support to the Senior Manager/Associate Director in ensuring procedural compliance with GCP standards and other… more
- Amgen (Washington, DC)
- …+ Experience working in a global, matrix organization. + Knowledge of Good Clinical Practices ( GCP ), FDA regulations and guidelines, and international regulatory ... world. In this vital role you will support Amgen-sponsored clinical trials worldwide. Reporting to the Senior Manager of...of R&D Supplier Governance, you will help ensure the quality and integrity of processes and data generated by… more
- GRAIL (Durham, NC)
- … Compliance will play a key leadership role in shaping and strengthening Grail's Clinical Quality Management System (CQMS) and advancing clinical compliance ... initiatives. + Revise, develop, and maintain procedures within the Clinical Quality Management System, leveraging lessons from...CFR Part 812 and Part 11]. + Experience managing GCP quality processes such as managing … more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ... teams for regulations impacting Clinical , Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and...Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring ... strategy, model, and operations as a key member of Clinical Quality program leadership team. **What you...Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical… more
- Lilly (IN)
- …operates. The purpose of the job is to ensure ExploR&D has adequate Good Clinical Practices ( GCP ) systems in place that are properly executed. Responsibilities ... appropriate, fit for purpose systems for ExploR&D to conduct GCP -regulated work, in accordance with the ExploR&D Quality...partnerships with external companies developing molecules in early phase clinical trials. The Sr. Director ExploR&D … more
- Regeneron Pharmaceuticals (Warren, NJ)
- … to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution ... studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment… more
- Bausch + Lomb (Harrisburg, PA)
- …global team members, other B&L departments (eg, R&D/Project Management, Clinical /Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, ... GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,...purposes. **POSITION REQUIREMENTS** **:** + Strong knowledge of Good Clinical Practices ( GCP ), clinical trials… more
- IQVIA (Durham, NC)
- …strategically to realize clinical project goals including setting and developing clinical strategies. + Ensure clinical quality delivery by identifying ... bringing new drugs to the market faster. The Associate Clinical Lead Director is a member of...compliance will be measured, monitoring and overseeing management of clinical quality issues. + Manage clinical… more
- Teleflex (Wayne, PA)
- Senior Director , Clinical Evidence Generation (REMOTE) **Date:** Jul 23, 2025 **Location:** Wayne, PA, US **Company:** Teleflex **Expected Travel** : Up to 10% ... make a difference in patients' lives. **Position Summary** The position of Sr. Director , Clinical Evidence Generation is a newly created position reflecting… more