- 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… 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 ... organizational processes. + Collaborate with cross-functional teams (eg, Regulatory, Quality Assurance , Lab Operations, Clinical Data Management,...CFR Part 812 and Part 11]. + Experience managing GCP quality processes such as managing … more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Alliance Vendor Relationship Manager Date: Jul 22, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva ... and new people to make a difference with. **The opportunity** The Associate Director , Alliance/Vendor Relationship Manager will be responsible for managing… more
- BeOne Medicines (San Mateo, CA)
- **General Description:** The Associate Director (AD), GCOE Learning and Development responsible for managing the governance, configuration, and optimization of ... Operations, Clinical Compliance, Clinical Monitoring, Clinical Trial Management, and/or Clinical Quality Assurance .) + Experience training on CTMS, TMF systems,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …aspirations. Join Gilead and help create possible, together. **Job Description** The Associate Director , Good Pharmacovigilance Practice (GVP) Audits, serves as ... Annual Audit Program. Reporting to the Head of GVP Audits, the Associate Director contributes to the strategic development and operational execution of… more
- e CancerCare (Fresno, CA)
- Purpose: The Director , Clinical Trials & Research, for CCARE Physicians, PC, is responsible and accountable for the daily operations and management of staff, of the ... compliance with all regulatory requirements and standards of good practice ( GCP ) related to the conduct of clinical research. Responsibilities/Essential Functions… more
- Walmart (Bentonville, AR)
- **Position Summary ** **What you'll do ** As a Director - Software Engineering for the Corporate Real Estate teams at Walmart, you will be instrumental in defining ... of robust, scalable, and efficient architectural solutions for the Associate campus experiences. In this role, you will be...efficiency across Walmart globally. **What you'll do:** As a director , you will be instrumental in defining the technical… more
- University of Utah (Salt Lake City, UT)
- …and contracts; assists in the development of case report forms. 16. Develops QA /QC processes and conduct quality control activities (field/study visits, data ... Title** PS Clinical Research Coord Sr. **Working Title** Sr. Clinical Research Associate **Job Grade** F **FLSA Code** Administrative **Patient Sensitive Job Code?**… more
- University of Utah (Salt Lake City, UT)
- …assigned to the job. E **ssential Functions** 1. Oversee, coordinate and conduct quality assurance reviews, including monitor and audit visits on cancer related ... knowledge regarding federal and state guidance, including Good Clinical Practice ( GCP ). **Problem Solving** Incumbent is responsible for assisting the University… more
- Guidehouse (Bethesda, MD)
- …all safety standards and protocols related to environment + Submit images of technical quality + Perform QA /QC procedures in accordance with the American Society ... will work under the general direction of a physician ( director ) within a unique clinical research environment as well...least EIGHT (8) years of sonographic experience or an associate 's degree in a health science program plus TEN… more