- Gilead Sciences, Inc. (Foster City, CA)
- …procedural documents, and quality and inspection readiness for Clinical Operations. The Associate Director will be a key member of the Connect GCP ... team and collaborate with Clinical Operations personnel to ensure quality , proactively identify risk, mitigate non-compliance, and support deviation management… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process 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
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Associate Director , Regulatory Job Profile Title Associate Director , ... Clinical Research Regulatory Job Description Summary With the oversight of the Director , the Associate Director for Regulatory Affairs will oversee the… more
- Bristol Myers Squibb (Madison, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . Job Description The Associate Director , RBQM - HOCT, ICN will mainly be responsible for ... developing the Quality Narrative at the study and/or ASSET and TA...regulatory compliance. **Required Competencies:** + Demonstrated applied knowledge of ICH/ GCP , regulatory guidelines/directives, clinical research processes and principles of… more
- Penn Medicine (West Chester, PA)
- …future each day. Are you living your life's work? **Summary** : + The Associate Director Oncology Research Operations reports directly to the Senior Director ... Community Impact at Penn Medicine Chester County Hospital0. The Associate Director works closely with the Physician...show vigilance in patient safety, protocol compliance and data quality . This employee must adhere to the requirements of… more
- Pfizer (Collegeville, PA)
- …SUMMARY** + The overall role of the Early Clinical Research Clinician/Clinician Scientist Associate Director is to support the development and execution of ... of concept (PoC) studies in a given therapeutic area. + The Clinician/Clinical Scientist Associate Director may be mentored by a more senior Early Clinical… more
- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director , Head, ICSR ... in the safety database and are reported according to ICH- GCP guidelines, Healthy Authority regulations and company SOPs, Work...PV Vendor processing ICSRs for Ascendis Products. + Performs Quality Checks of processed ICSRs and provides feedback to… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …outsourcing, oversight and risk-based data management strategies, standards and processes. The Associate Director , Data Management will bring deep knowledge of ... management strategies, processes, and standards in alignment with Good Clinical Practices ( GCP ) and applicable regulatory guidelines (eg, FDA, EMA, ICH). * Oversees… more
- Pfizer (Bothell, WA)
- **Job Summary** The Associate Director , Clinical Development Medical Director : + Is accountable for the medical & scientific integrity of the study and the ... clinical and medical colleagues, clinical operations, and other functional lines. The Associate Director , Clinical Development Medical Director is… more