- 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...ways of working. + Partner with R&D Quality and GCP Compliance Management to develop GCP… 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...guidelines including the management of significant/complex quality issues and compliance activities. * Extensive experience with participating in, and… 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
- Lilly (Indianapolis, IN)
- …for people around the world. **Position Overview:** The PR&D Quality System Associate Director provides critical leadership, oversight, and cross functional ... the PR&D Quality System (QS) are well managed. The PR&D Quality System Associate Director partners cross functionally with the business to implement key… more
- Takeda Pharmaceuticals (Boston, MA)
- …delivery, and deployment of training; monitors and tracks employee training compliance with the LMS. + Oversees the coordination, including the collection, ... tracking, and trending of key PV Compliance metrics for the monthly cross-functional Compliance ...of FDA/EU regulations, and ICH guidelines for GVP and GCP with practical experience in the interpretation and implementation… 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, implementing, ... requirements applicable to the conduct of clinical trials. The Associate Director , Quality will partner with key...CDS organization to ensure clinical trials are conducted in compliance with Gilead procedures, GCP and applicable… 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...resource for the department, ensuring scientific integrity and regulatory compliance in the application of statistical methodology to clinical… 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 ... of products in development. + Through coordination with Ascendis GCP and PV Compliance team will provide...team (specifically from: Talent Acquisition Partner or Human Resources Director ) is not allowed. If this occurs your ownership… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
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