- Bristol Myers Squibb (Madison, NJ)
- …will provide direct technical and quality compliance oversight of the commercial program (vector, gene editing and cell therapy projects) to ensure regulatory ... compliance of GMP operations in support of the program .The PQL must drive alignment across cell therapy programs that are appropriate for a commercial program … more
- Bristol Myers Squibb (New Brunswick, NJ)
- …focus on developing safe, economical, sustainable, and robust processes to support clinical trials and the launch of new medicines across various drug modalities ... execution of experiments that are in line with portfolio program strategy. Based on experimental learnings, you will be...the transition of such processes from our labs to clinical supply, to regulatory filings and manufacturing vendors. As… more
- Bristol Myers Squibb (Princeton, NJ)
- …biopharmaceutical industry, across a spectrum of assets in early and late clinical development as well as experience with preclinical staged assets. The candidate ... competitive BD processes + Keep current on scientific / clinical data trends in biopharma in core therapeutic areas...+ US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to… more
- Bristol Myers Squibb (Madison, NJ)
- …studies, and developing, validating, and analyzing health economic models and clinical outcomes assessment measures. The Director partners closely with key ... not limited to field HEOR, Pricing & Access Strategy, Medical Affairs, Clinical Development, Marketing, PReP Team, Center of Observational Research and Data… more
- Bristol Myers Squibb (Princeton, NJ)
- …with key stakeholders including, but not limited to, US Commercialization, Clinical Development teams, among others. **Key Responsibilities:** + Provide strategic, ... areas outside of medical including marketing, sales, access, legal, regulatory, clinical operations, and research and development + Ensure US medical strategies,… more
- Bristol Myers Squibb (Summit, NJ)
- …the production of personalized cell therapy products for both global clinical trials and commercial supply. Potential areas of responsibility include providing ... and/or drug product life cycle sustainability, managing CPV and process monitoring program , and support development and lifecycle management of MBR and EBR. These… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …Activities include those associated with product stability strategy, stability program requirements, stability sample management, preparation, review and approval of ... + The Associate Director Stability is accountable for the stability commercial program for large molecules Drug Substances and Drug Products. + Accountable for… more
- Bristol Myers Squibb (Madison, NJ)
- …PhD, NP) preferred with 15+ years of executive management experience in clinical development and medical affairs in the pharmaceutical industry, with an emphasis ... Affairs experience. + Disease area expert in Immunology + Clinical or Academic Experience (Patient Facing) is desirable +...+ US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to… more
- Bristol Myers Squibb (Princeton, NJ)
- …with oncology asset level matrix teams, including market access, clinical development, medical affairs, regulatory, biostatistics to ensure full alignment ... and develop strong partnership with external key opinion leaders in clinical , health economics, and outcomes research + Manage prospective observational… more
- Bristol Myers Squibb (Princeton, NJ)
- …additional documents and activities such as: Dear Health Care Professional letters, Clinical Overview for Type II variation and coordinate expert reports. + Provide ... clinical trial expertise for existing evidence generation studies or...+ US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to… more
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