- Gilead Sciences, Inc. (Foster City, CA)
- …team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve ... Regulatory Affairs or other relevant industry experience. + Degree in a scientific field is preferred. Specific Job Responsibilities: + Responsible for preparing… more
- University of Colorado (Aurora, CO)
- **Open Rank Associate to Assistant Professor - Clinical Pathology** **Description** **University of Colorado Anschutz Medical Campus** **Department: Pathology** ... **Job Title: Open Rank - Associate to Assistant Professor Clinical Pathology** **Position...Clinical Pathology faculty, laboratory staff, and trainees. + Clinical laboratory director responsibilities within the scope… more
- GRAIL (MD)
- …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome ... Maintain up-to-date knowledge of applicable regulatory requirements and relevant scientific /technical developments. + Identify regulatory risks and propose alternative… more
- Kelly Services (South San Francisco, CA)
- Kelly(R) Science & Clinical is seeking an Associate Director / Director of Drug Substance Manufacturing for a direct hire opportunity with a leading ... Senior Director , $275,000 - $320,000 **Overview** As Associate Director / Director , Drug...(R) Science & Clinical ? Kelly Science & Clinical is your connection to premier scientific … more
- Merck (West Point, PA)
- …+ Setting future strategies and sponsoring new technologies. + Responsible for scientific oversight of work outsourced to Clinical Research Organizations (CROs) ... and ensure safety and quality of our products. The Director of Vaccines Potency in Analytical Research & Development...be responsible for a team of 10-15 senior and associate level scientists. The position is accountable for developing… more
- Bristol Myers Squibb (Princeton, NJ)
- …Commercial partners of the team include the Lung Commercial Strategy, Scientific Engagement, Events and Meetings Center of Excellence, Strategy & Operations, ... Medical Matrix, Therapeutic Areas, and Regions **Qualifications & Experience** + Advanced scientific degree (PharmD, Advanced Nursing Degree, PhD). + Minimum of 3+… more
- AbbVie (North Chicago, IL)
- …ensure consistent preparation of CMC regulatory submission documents of high scientific and technical quality that are compliant with global regulatory requirements. ... ensuring that the CMC submission strategy is aligned closely with the clinical /regulatory development strategy and provides drug development experience and advice to… more
- Takeda Pharmaceuticals (Boston, MA)
- …(from statistics, programming, outcomes research and epidemiology, quantitative clinical pharmacology, digital strategy, library sciences and data ... with our quantitative skills. We design efficient trials, contribute to clinical development strategies, perform high quality statistical analyses, and pursue… more
- Takeda Pharmaceuticals (Boston, MA)
- …improvement + Lead CPMQ continuous improvement initiatives to enable optimization of clinical and safety quality compliance activities. + Provide expert advice and ... metrics for CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and… more
- Sumitomo Pharma (Topeka, KS)
- …or follow us on LinkedIn. **Job Duties and Responsibilities** + Lead on clinical studies and manage/provide training to team members when needed. + Contribute and ... SAS/SQL and SAS/ODS. + Interact with Statisticians and other clinical teams, perform ad hoc analysis and generate +...plus. + BS/MS or equivalent in Statistics, Math or Scientific Discipline The base salary range for this role… more