- Merck (Rahway, NJ)
- …GMP capability build for the production of clinical supplies of bulk biologic drug substance at a state-of-the-art Next Generation Biologics (NGB) facility at our ... time the incumbent will manage a small organization of 3-4 exempt and non -exempt employees to support bulk clinical manufacturing of biologic drug substances,… more
- Bristol Myers Squibb (Princeton, NJ)
- …activities build upon the early work, additionally exploring mechanisms of response/ non -response, rational drug combinations and product differentiation. The ... a department within the Research organization that facilitates the transition of drug candidates from early to late-stage clinical development, their approval and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …with 10+ years' relevant experience. + 4+ years' experience in prescription drug labeling. + Significant regulatory experience in the biopharma industry is strongly ... with one or more Gilead therapeutic areas and varying stages of drug development is strongly preferred. **Knowledge & Other Requirements** + In-depth knowledge… more
- Charles River Laboratories (Rockville, MD)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... and safety assessment services, both Good Laboratory Practice (GLP) and non -GLP, to support clients from target identification through preclinical development.… more
- Gilead Sciences, Inc. (Foster City, CA)
- …projects and teams with responsibilities related to clinical trials or other drug development activities + Familiar with the practice of recording and monitoring ... ICH) and related industry standards and trends + Through knowledge of the drug development process, including all key functions involved in the various stages of… more
- Amneal Pharmaceuticals (Bridgewater, NJ)
- …and actively represent Legal on the company PARC to review promotional/ non -promotional materials and strategies covering multiple topics (disease awareness, patient ... FDA regulations, OIG guidance, PhRMA Code, Federal healthcare programs, state drug transparency laws, HIPAA/privacy, etc.). + Negotiate, draft, and review market… more
- Truist (Charlotte, NC)
- …policies and procedures to effectively manage the risk of GAAP non -compliance by reflecting new accounting pronouncements or guidance, improving clarity or ... you will also learn more about the specific benefits available for any non -temporary position for which you apply, based on full-time or part-time status, position,… more
- Lilly (Indianapolis, IN)
- …handling + Communicate complex technical information to both technical and non -technical stakeholders and influence decision making at senior leadership level. + ... that enable Digital Supply Chain + Experince in upskilling both technical (IT) and non technical (business) resources in the design principles and use of SAP, WM and… more
- BeOne Medicines (San Carlos, CA)
- …biology + Extensive (4+ years) project or program experience in preclinical drug discovery and clinical biomarker, leading large complex multi-stakeholder projects + ... Strong understanding of the global drug discovery and development, clinical biomarker and translational science strategy development, with ability to lead program… more
- Lilly (Indianapolis, IN)
- …time pressure. + Skilled in searching out information from both traditional and non -traditional sources, all within the guidelines of our policy. Ability to work ... pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (eg, healthcare and/or dependent day care… more