- 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
- 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
- Bristol Myers Squibb (Princeton, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . The position is for an Associate Director / Investigator in the Compliance & Ethics ... will range in routine to complex in nature. The Associate Director / Investigator will plan, conduct, and...Director / Investigator will plan, conduct, and manage internal Compliance & Ethics investigations related to reported violations of… 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
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- We are seeking a Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the ... of study data of a clinical development program. The Associate Director leads in a matrix environment...compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical… more
- System One (Tarrytown, NY)
- Job Title : Temp - Associate Director , Aggregate Reporting, GPS Type: Contract Compensation: $85 - $100 hourly (dependent on experience) Contractor Work Model: ... + Ability to interpret clinical data to support benefit-risk assessments. Temp - Associate Director , Aggregate Reporting, GPS + Submit Candidate + This position… 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
- 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
- J&J Family of Companies (Irvine, CA)
- …States of America **Job Description:** We are searching for the best talent for an Associate Director of Clinical Research located in Irvine, CA and Santa Rosa, ... CA. Purpose: This Associate Director Clinical Research will be leading...internal/external stakeholders (deliver on time, within budget and in compliance with regulations and SOPs); + Leads a team… more
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