- Lilly (Durham, NC)
- …the charge in shaping the future of manufacturing at Eli Lilly? As an Associate Director of Operations, you'll be at the forefront of this exciting journey. In this ... documentation including procedures, deviation investigations, technical reports, change controls, regulatory submissions, validation protocols and summary reports, etc. +… more
- AbbVie (Irvine, CA)
- …committed to providing the most comprehensive science-based product offerings available. The Director I will provide direction and oversight to the design, planning ... author, edit and review key section of research protocols, reports and regulatory submissions. Responsibilities: + Based on strong medical and scientific experience,… more
- Fresenius Medical Center (Vancouver, WA)
- …programs in an assigned area ensuring compliance with established company and regulatory guidelines and procedures in order to provide high quality dialysis services ... of area while ensuring compliance with all pertinent company policies and regulatory requirements. PRINCIPAL DUTIES AND RESPONSIBILITIES: + Directs and oversees the… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and help create possible, together. **Job Description** **POSITION OVERVIEW:** As Director of Clinical development in the Inflammation/Fibrosis therapeutic area, you ... analysis plans, study reporting, and clinical development input into regulatory documentation, publications, and scientific presentations. Scope may include phase… more
- Amgen (Washington, DC)
- …on Amgen's mission to serve patients around the world. As the Senior Director of Biostatistics in Biosimilar Development provides strategic statistical input to and ... in Amgen's Biosimilar Development. + Ensures excellent statistical input into regulatory strategies, presentations and scientific reports for clinical trial, … more
- Katecho (Des Moines, IA)
- Surmasis Pharmaceutical - Director of Quality | M-F | Pay Based on Experience + + Job Tracking ID: 512885-901176 + Job Location: DES MOINES, IA + Job Level: Mid ... all products manufactured by the organization meet customer specifications and regulatory requirements and achieve superior quality and reliability levels. This… more
- Corewell Health (Grand Rapids, MI)
- Job Summary The Director Risk Adjustment Prospective Operations & Risk Mitigation is the thought leader role responsible for ensuring the complete and accurate ... risks and will implement the necessary procedures to ensure compliance with regulatory standards. This position will develop and manage key performance indicators… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Senior Statistical Project Leader ( Director ) **Location:** Cambridge, MA, Morristown, NJ **About the Job** Are you ready to shape the future of ... medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Join our **Biostatistics Immunology &… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Executive Medical Director , Hematology, will provide overall clinical scientific leadership for the C5 program and have responsibility for our clinical ... scientific knowledge applicable to hematology clinical research. The Executive Medical Director , Hematology reports directly to the SVP, Hematology. **A typical day… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …as a general understanding of important topics including clinical trial design, drug development, regulatory decision making and public policy. + Responsible ... **Job Summary** The Senior Director , CNS Communications, is the senior strategic communications...programs, as well as planning around key data announcements, regulatory milestones and launch planning for late-stage pipeline candidates.… more