- Takeda Pharmaceuticals (Boston, MA)
- …company to inspire you and empower you to shine? Join us as an Associate Director , GCP Excellence in Clinical Trials based remotely reporting ... to the Director , GCP Excellence in Clinical Trials. At...and inspections. + Develop, lead and oversee strategies for GCP quality and inspection plans, collaborating with… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Associate Director , Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is ... responsible for the effective management of GCP , GVP and GLP inspections. The GDQIM IML will...Investigator Site Preparation Visits, in collaboration with the GD Quality Assurance (GDQA) team and other relevant functional groups.… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** **Summary** The Associate Director , Quality will be responsible for designing, ... System (QMS). This role requires an in-depth knowledge of GCP and understanding of regulatory requirements applicable to the...requirements applicable to the conduct of clinical trials. The Associate Director , Quality will partner… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. **Position Overview:** The PR&D Quality System Associate Director provides critical leadership, oversight, and ... Quality System (QS) are well managed. The PR&D Quality System Associate Director partners...supervision. + Strong working knowledge of cGMP requirements and GCP regulations. + Strong leadership and teamwork skills. +… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ... 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)
- …is true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ... and Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and … more
- IQVIA (Durham, NC)
- **Job Level: Associate / Director of Biostatistics,** **Early Phase Pharmacodynamics** **Location:** **Home-based in the US or Canada** **(East Coast Preferred)** ... **Job Overview:** As an ( Associate ) Director , you will liaise with cross-functional..., you will liaise with cross-functional teams to drive quality statistical planning, analysis, and reporting in support of… more
- J&J Family of Companies (Titusville, NJ)
- …https://www.jnj.com/innovative-medicine **We are searching for the best talent for an Associate Director , Portfolio Lead Clinical Programming within C&SP Group ... to be located in Titusville, NJ.** **Purpose:** An Associate Director , Portfolio Lead is a highly experienced individual with expert understanding of programming… more
- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. Associate Director , Global Patient Safety Medical Science reports to Head of GPS ... that all safety reports received from any source are reviewed according to ICH- GCP guidelines, regulatory requirements and company SOPs and procedures. + Performs … more
- BeOne Medicines (San Mateo, CA)
- …with CTOMs; including but not limited to adherence to monitoring SOPs, GCP guidelines, country-specific regulations, and general quality and risk-based ... the performance and results of multiple related teams Supports SR Director to develops departmental plans, including business, production and/or organizational… more
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