- Bristol Myers Squibb (Princeton, NJ)
- …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... in their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** The… more
- AbbVie (Florham Park, NJ)
- …of work may include clinical trials, patient safety, and global medical affairs . The Associate Director works in partnership with experts in multiple ... IL; San Francisco, CA; Irvine, CA; Florham Park, NJ The Associate Director , Statistics provides statistical leadership for clinical development and life-cycle… more
- AbbVie (Florham Park, NJ)
- …of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple ... Director , Statistics - Immunology provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific… more
- J&J Family of Companies (Titusville, NJ)
- …expertise with multiple components of drug development, such as translational research, clinical studies, or regulatory interactions. + Working knowledge of ... of Johnson & Johnson is recruiting for a Senior Director , R&D Data Science & Digital Health - Oncology,...audience. + Prior experience serving on multifunctional teams delivering clinical trials in an R&D or Medical Affairs… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …and guide product strategy -- May include cross-functional collaboration with R&D, Medical Affairs , Market Access, Regulatory Affairs and Marketing + ... reimbursement submissions, payment issues, policy statements, HTA submissions + Medical/Scientific Affairs : clinical study development support and execution +… more
- Bristol Myers Squibb (Madison, NJ)
- …for Market Access objectives + Work as part of cross-functional teams-including clinical development, medical affairs , regulatory , and biostatistics-to ... Research Scientist roles. You will define and oversee the execution of clinical outcomes assessment (COA) strategies and implementations for the rigorous development… more
- Bristol Myers Squibb (Princeton, NJ)
- …of the biopharma drug development and commercialization process. + Experience in clinical research and development, or medical affairs in Psychiatry/Neurology is ... in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , US Medical Neuropsychiatry position works in the US Medical… more
- Sumitomo Pharma (Trenton, NJ)
- …strategic business questions and relevant cross-functional stakeholders, including in Commercial, Clinical Development, Medical Affairs , Regulatory , Sales ... LinkedIn (https://c212.net/c/link/?t=0&l=en&o=4190475-1&h=2504638834&u=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fsumitomo-pharma-america%2F&a=LinkedIn) . **Job Overview** The **Associate Director , Competitive Intelligence** will seek out, collect,… more
- J&J Family of Companies (Titusville, NJ)
- …via matrix interactions includes individuals from TA strategy, GCSO, global regulatory affairs , project management, finance, legal, quality assurance, quality ... products including Excel and Word + Experience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to ... **Associate Director , Small Molecule Analytical Development** + Lead and...knowledge of the drug development lifecycle, including preclinical and clinical stages, regulatory requirements, and quality standards.… more