- Genmab (NJ)
- …feel like a fit? Then we would love to have you join us!The Global Regulatory Labeling , Policy and Intelligence Associate Director will primarily be ... of labeling documents according to internal SOPs and external regulatory requirements.Prepare submission-ready labeling documents; Maintain and track … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and ... applications/supplements & variations (eg, NDA, BLA, MAA). This position authors regulatory documents where necessary with supervision. This position conducts … more
- Merck & Co. (Rahway, NJ)
- …of clinical trial s .- GCS is accountable for the planning, sourcing, labeling , packaging and delivery of clinical supplies to clinical sites globally. The GCS ... as a lead GCS Planning program representative ) such as clinical development, regulatory , quality and other supply chain areas to negotiate timelines ,- strategies… more
- Bristol Myers Squibb (Princeton, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director of WW Medical Neuroscience, Neuro degeneration Medical ... including WW Commercial, Research and Development, Global Drug Development, HEOR, Regulatory Affairs, and other global medical stakeholders. This position reports to… more
- Bristol Myers Squibb (Princeton, NJ)
- …integration points across US functional and commercialization areas to ensure alignment. The Associate Director will report to the Senior Director, US Medical ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , US Medical Neur opsychiatry position works in the US… more
