- Insmed Incorporated (San Diego, CA)
- …for Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director , EDC Programming will lead and oversee EDC ... implementation of EDC systems to support clinical trials, ensuring data quality, compliance , and efficiency throughout the study lifecycle. The AD, EDC Programming… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …is a global role that will cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the ... across the global safety organization. The incumbent will ensure regulatory compliance , promote best practices, foster a culture of continuous improvement in… more
- Merck & Co. (North Wales, PA)
- …Compliance Program Development, Crisis Management, Cross-Cultural Awareness, Detail-Oriented, Global Compliance , Good Clinical Practice ( GCP ), IS Audit, Issue ... governed by this role. Strategic duties involve providing proactive assessments of compliance culture and governance through input to the GRACS Compliance … more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …(TPP) development, due diligence projects, and clinical-regulatory compliance . ResponsibilitiesEssential Duties and Responsibilities Clinical Development: Design ... and execute clinical trials for respiratory products, ensuring compliance with regulatory requirements.Collaborate with cross-functional teams to develop study… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Senior Director of Clinical Operations will manage clinical operations staff to ensure ... ongoing collaboration and communication with internal stakeholders. Detailing The Senior Director will ensure a robust communication plan including status and timing… more
- Amgen (Washington, DC)
- …support to the Senior Manager/ Associate Director in ensuring procedural compliance with GCP standards and other regulatory requirements across R&D. + Act ... transform the lives of patients while transforming your career. ** GCP Quality Compliance Manager** **What you will...experience OR + Bachelor's degree and 4 years of Quality/ Compliance /Process Management experience OR + Associate 's degree… more
- GRAIL (Menlo Park, CA)
- …support Grail's partnerships with pharmaceutical companies for companion diagnostic (CDx) tests. The Associate Director , Clinical Compliance will play a key ... System, leveraging lessons from inspections, audits, and emerging clinical compliance trends, in both GCP and CDx...and emerging clinical compliance trends, in both GCP and CDx domains. + Contribute to, implement, and… more
- Amgen (Washington, DC)
- …Suppliers for Amgen sponsored clinical trials + Monitoring and evaluating Supplier compliance and data quality + Tracking corrective actions in relation to ... external partners, including study teams, functional leads, procurement, quality, compliance , and suppliers + Support business functions with evaluation, selection,… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
- Takeda Pharmaceuticals (Boston, MA)
- …on quality compliance activities. + Provide guidance and support to GCP , PV Health Authority inspections including logistics. + Present insights to the health ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
Related Job Searches:
Associate,
Associate Director,
Compliance,
Director,
Director GCP,
GCP,
GCP Compliance