- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …responsibility to support the VP, Medical Affairs in providing medical, scientific and technical customer-focused leadership and strategic perspectives across the ... Specimen Management (SM) business unit, as well as acting as...and evidence generation plans as well as publication and scientific exchange plans to contribute to product development, meet… more
- Sanofi Group (Morristown, NJ)
- …PM DICT will be responsible for the delivery and growth the DICT Project Management Office (PMO) and supporting the DICT country leads in executing on DICT ... of and maintenance of D&I in clinical trials Project Management Office (PMO). + Act as the key interface...change plan, implements them and measures progress. + **Intermediate Data Analytics (& Digital Skills)** : Uses the systems,… more
- J&J Family of Companies (Titusville, NJ)
- …for the early development portfolio across Neuroscience and provide line management for CDTL's leading early development programs. A key operating principle ... with the Neuroscience TA leadership to develop comprehensive clinical and scientific de-risking strategies for the drug candidate(s) to move quickly into… more
- Bristol Myers Squibb (Princeton, NJ)
- …deadlines. **Education / Experience Requirements** + Bachelor's degree required; advanced scientific degree preferred (Masters, PhD, PharmD, BSN, etc.) with at least ... Regulatory Agencies globally for drug development and approval. + Understanding of scientific content and complexities and good knowledge of drug development is… more
- Dr. Reddy's Laboratories (Princeton, NJ)
- …drive Medical Affairs strategies and be responsible for accurate patient safety data . Provide oversight on medical information services and support in providing ... procedures to be documented and set up. Establish the pharmacovigilance Quality Management System and achieve compliance with US regulatory requirements + Review… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …the discovery and development cycles within R&D and an ability to understand scientific discussions at a level of proficiency sufficient to perform the role. Proven ... to work cross-functionally. **Job Description** . Develop and maintain thorough scientific and industry/trend knowledge of Neph/Imm therapeutic area along with… more
- Sanofi Group (Morristown, NJ)
- …track record from scientific publications in core COA disciplines such COA data analyses and/or creation or validation of new COAs and/or COA endpoint strategy ... scientists. + The Senior COA Lead is accountable for scientific quality of activities and deliverable in their defined...technical skills :** + Appetite for innovation and change management + Ability to interact and manage external and… more
- Bristol Myers Squibb (Princeton, NJ)
- …and CDx studies, including CRO oversight, assay transfer and validation, sample/ data logistics, and discrepancy reconciliation to ensure timely, compliant execution. ... + Provide bioanalytical project management for clinical studies, managing critical reagents and timelines for deliverables. + Monitor operational risks and… more
- Sanofi Group (Morristown, NJ)
- …strategy for assigned products, including those in clinical development, life cycle management (LCM), and the marketed portfolio. This role leads the creation and ... update of core labeling documents (eg, Company Core Data Sheet) and regional labeling (eg, US Prescribing Information, EU SmPC), ensuring alignment with regulatory… more
- Sanofi Group (Morristown, NJ)
- …the core product labeling for products in development as well as for lifecycle management of products. + May serve as a regional/local regulatory lead and point of ... the authoring of the briefing document focused on the strategy and scientific content, leading the team through meeting preparations and moderating the meeting… more