- Sanofi Group (Morristown, NJ)
- …(new products or marketed products) in collaboration with all Global Regulatory Affairs entities. + Participate in Change Control assessment. + Guarantee strong ... to define the future submission strategy; in collaboration with R&D functions, Industrial Affairs , Global Regulatory Affairs . + Coordinate the submission of CMC… more
- Grifols Shared Services North America, Inc (Trenton, NJ)
- …ensure alignment of technical activities with regulatory strategies. + Utilizes scientific training when interfacing with Management of technical areas and project ... around emerging/changing regulatory requirements. + Writes documents with complex scientific information for regulatory submissions. + May supervise staff +… more
- J&J Family of Companies (Titusville, NJ)
- …development for Alzheimer's Disease projects. They will provide strategic, clinical, and scientific support and be accountable for the execution of the clinical ... development team (CDT). **ESSENTIAL FUNCTIONS:** + Provides active medical and scientific contribution to a matrixed cross-functional Compound Development Team and… more
- Bristol Myers Squibb (Princeton, NJ)
- …will be part of a team dedicated to supporting legal, policy & government affairs and commercial teams by conducting detailed US or Global policy impact modelling ... pharma pricing policy strategies, including MAx, Global Policy & Government Affairs , Finance, and Business Insights & Technology. The position requires sophisticated… more
- J&J Family of Companies (Raritan, NJ)
- …Sub** **Function:** Clinical Development & Research - MD **Job Category:** Scientific /Technology **All Job Posting Locations:** Raritan, New Jersey, United States of ... reports. + Acts as the clinical functional head for providing active scientific contributions to a cross-department compound development team. + Works in close… more
- Sanofi Group (Morristown, NJ)
- …a positive, collaborative mindset. + Take an active part in the scientific challenges involved in early clinical development, which require a scientifically ... (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area Research & Development… more
- Merck (Rahway, NJ)
- …is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates. The incumbent ... case report forms, data analysis plans, final study reports, scientific presentations, and publications + Responsible for study-related contracting, budgets,… more
- Bristol Myers Squibb (Princeton, NJ)
- …Therapy Medical organization. We have an opening for an Associate Director, US Medical Affairs , Cell Therapy, which will report directly to the Senior Director of US ... advice to conduct the review of promotional materials for scientific /medical validity. They will also serve as the US...to promote the interests and initiatives of US Medical Affairs + Conducts business in accordance with BMS Values… more
- Regeneron Pharmaceuticals (Warren, NJ)
- The Senior Manager Statistical Programming for Medical Affairs provides timely support to the Medical Affairs project team on all programming matters according ... and annual reports. The Senior Manager Statistical Programming for Medical Affairs may serve as the statistical programming lead for indication(s)/product(s) within… more
- AbbVie (Florham Park, NJ)
- …areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple ... leadership for design, analysis and reporting for clinical or other scientific research programs. Independently develop protocols and statistical analysis plans. +… more