- Insmed Incorporated (San Diego, CA)
- …Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewReporting to the Executive Director of Clinical Quality Assurance, the Director ... and regulatory compliance related to GCPs, acts as quality lead on the gene therapy clinical ...with cross functional working groups to identify and mitigate GCP quality and compliance issues.Supports the evaluation… more
- Eisai, Inc (Nutley, NJ)
- …environment and make a difference. If this is your profile, we want to hear from you. Director , Clinical Quality Assurance The Director , Clinical ... management system. This role is responsible for Good Clinical Practice ( GCP ) oversight, and for assuring...Eisai Salary Transparency Language:The base salary range for the Director , Clinical Quality Assurance is… more
- Merck & Co. (Rahway, NJ)
- …organizations ( as a lead GCS Planning program representative ) such as clinical development, regulatory, quality and other supply chain areas to negotiate ... / portfolio management. - Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. - Preferred Experience and… more
- Merck & Co. (North Wales, PA)
- …clinical data/medical protocol deviations in collaborations with the Clinical Director .Other responsibilities include:Collaborating cross-functionally in the ... protocol in collaboration with Data Management/Programming.Collaborating cross-functionally to monitor clinical data to ensure quality , completeness, and… more
- Merck & Co. (Rahway, NJ)
- … clinical data/medical protocol deviations in collaborations with the Clinical Director . Other responsibilities include: Collaborating cross-functionally in ... in collaboration with Data Management/Programming. Collaborating cross-functionally to monitor clinical data -to ensure quality , completeness ,... research regulatory requirements (e . g . , GCP and ICH) Ability to manage multi e competing… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …global clinical regulations and guidance. + Support the development of GCP Audit material/insights for quality forums and management reviews. _Training & ... aspirations. Join Gilead and help create possible, together. **Job Description** Gilead R&D Quality is a phenomenal place to develop your skills and expertise. Our… 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 ... quality /compliance role (eg, Quality Management, Quality Assurance etc.), or in a Clinical ...role with expertise and/or transferable skills related to Good Clinical Practice ( GCP ), and/or Good Pharmacovigilance Practice… more
- Amgen (Washington, DC)
- …+ Experience working in a global, matrix organization. + Knowledge of Good Clinical Practices ( GCP ), FDA regulations and guidelines, and international regulatory ... world. In this vital role you will support Amgen-sponsored clinical trials worldwide. Reporting to the Senior Manager of...of R&D Supplier Governance, you will help ensure the quality and integrity of processes and data generated by… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ... teams for regulations impacting Clinical , Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and...Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring ... strategy, model, and operations as a key member of Clinical Quality program leadership team. **What you...Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution ... studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment… more
- Bausch + Lomb (Harrisburg, PA)
- …global team members, other B&L departments (eg, R&D/Project Management, Clinical /Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, ... GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,...purposes. **POSITION REQUIREMENTS** **:** + Strong knowledge of Good Clinical Practices ( GCP ), clinical trials… 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 ... Assures compliance with all regulatory requirements and standards of good practice ( GCP ) related to the conduct of clinical research. Responsibilities/Essential… more
- Teleflex (Wayne, PA)
- Senior Director , Clinical Evidence Generation (REMOTE) **Date:** Jul 23, 2025 **Location:** Wayne, PA, US **Company:** Teleflex **Expected Travel** : Up to 10% ... make a difference in patients' lives. **Position Summary** The position of Sr. Director , Clinical Evidence Generation is a newly created position reflecting… more
- Walgreens (Deerfield, IL)
- **Job Description:** **Job Summary** The Director , Clinical Quality Assurance Management for the RWE Clinical Trial business will be responsible for the ... issues to ensure business is performing to Good Clinical Practice ( GCP ) standards. This role will...CFR and ICH guidelines + Significant experience with managing clinical quality activities and in-depth knowledge of… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Medical Director , Clinical Development should be a...They will serve as Scientific and Medical Lead for clinical trials in the CDP according to GCP ... from CSCs * Accountable, along with CTM, for timely clinical trial execution and quality of deliverables...Clinical Team compliance with FDA, EMEA, ICH and GCP guidelines * Is the primary clinical … more
- Takeda Pharmaceuticals (Boston, MA)
- …be empowered to take charge of your future at Takeda. Join us as the Executive Director of Clinical Operations reporting to the Head of Global Clinical ... vital contributor to our inspiring, bold mission. The Executive Director of Clinical Operations will act as...and contingency planning for clinical programs and clinical studies. Accountable for on-time, high- quality and… more
- UCLA Fielding School of Public Health (Los Angeles, CA)
- Associate Director of Clinical Theranostics Research, Dept of Mol & Med Pharmacology Apply now to Associate Director of Clinical Theranostics Research, ... of California, Los Angeles (UCLA) invites applications for the position of Associate Director of Clinical Theranostics Research at the Assistant or Associate… more
- Teleflex (Minneapolis, MN)
- Director , Clinical Evidence Generation (REMOTE) **Date:** Jul 11, 2025 **Location:** Minneapolis, MN, US **Company:** Teleflex **Expected Travel** : Up to 10% ... to develop a culture of teamwork and results. The position of Director , Clinical Evidence Generation requires an experienced individual with demonstrated… more
- Regeneron Pharmaceuticals (Warren, NJ)
- The Senior Director of Clinical Data Operations is a key contributor to the operational vision, direction and strategy for the Data Management line function ... streamline external data integrations and improve data availability and quality to accelerate clinical data insights and...clinical data insights and decision making. The Senior Director of Clinical Data Operations is essential… more
