- Amgen (Washington, DC)
- …continuous improvement. + Provide hands-on support to the Senior Manager/ Associate Director in ensuring procedural compliance with GCP standards and other ... 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
- Lilly (IN)
- …approach to healthcare. For more information, visit www.avidrp.com . **Job Overview:** The Associate Director , Clinical Operations Quality Assurance is an ... Avid Quality Assurance (QA) function, ensuring the GCP Quality Management System (QMS) is well-defined,...collaboration with Avid Clinical Operations and Imaging Operations, the Associate Director of Clinical Operations QA ensures… more
- Actalent (Frederick, MD)
- …Assurance clinical operations. The Associate Director of QA will oversee quality for GCP , GLP, and PV operations, a fast-paced cell therapy environment. ... Description Quality Assurance Director with extensive experience...Practice (GVP) vendors and systems. * Prepares and negotiates Quality Agreements with vendors. * Manages study, GCP… more
- Amgen (Washington, DC)
- …to the Senior Manager of R&D Supplier Governance, you will help ensure the quality and integrity of processes and data generated by service suppliers for these ... sponsored clinical trials + Monitoring and evaluating Supplier compliance and data quality + Tracking corrective actions in relation to monitoring issues and audit… more
- GRAIL (Durham, NC)
- …Grail's partnerships with pharmaceutical companies for companion diagnostic (CDx) tests. The Associate Director , Clinical Compliance will play a key leadership ... 14155, IVDD/IVDR), US [21 CFR Part 812 and Part 11]. + Experience managing GCP quality processes such as managing Quality Events and CAPAs; and participating… 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
- Regeneron Pharmaceuticals (Warren, 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...maintaining compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical… more
- Ascendis Pharma (Palo Alto, CA)
- …We offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , PV Vendor Management Team reports to the Director , Head, ... of PV Vendor Management by contributing to the Vendor Quality Agreements + Accountable for maintaining oversight over Source...of CAPAs as necessary + Work Closely with Ascendis GCP /PV Compliance team and Commercial organization as required to… more
- ThermoFisher Scientific (Las Vegas, NV)
- …find cures for cancer. Due to continued growth, we are looking to appoint an Associate Medical Director at the Las Vegas Clinical Research Unit. This role is ... an office-based position for a motivated Physician. The Associate Medical Director serves as the physician...being conducted under all applicable laws, regulations and per ICH- GCP guidelines in the organization's Clinical Research Unit (CRU).… more