- Merck (North Wales, PA)
- …**Specifically, the Senior Director may be responsible for:** + Providing scientific and medical leadership for strategic alliances and Co-partnership opportunities. ... closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …**Who is USP?** The US Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's leading health and science experts ... for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global… more
- Lilly (Indianapolis, IN)
- …is an experienced clinical trialist who will be responsible for the clinical and scientific execution of global clinical programs. They will play a key role in ... insight into clinical development programs both externally and internally (eg, Medical Affairs , Commercial, CROs, etc.). They will provide clinical / scientific … more
- AbbVie (Irvine, CA)
- …high-quality clinical data supporting overall botulinum toxin and aesthetic franchise scientific and business strategy. Responsibilities: + Manages the design and ... the overall product development plan based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers,… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …support of BD's molecular and point-of-care diagnostic platforms. + Execute strategic scientific and educational initiatives aligned with medical affairs and ... Medical Science Liaison (MSL) II, you will serve as a manager and scientific expert, and strategically support the communication of medical scientific … more
- J&J Family of Companies (Irvine, CA)
- …Clinical R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs , Regulatory Affairs , Health Economics and Market Access, R&D, ... project budgets to ensure adherence to business plans. + Leads clinical scientific discussions with regulatory agencies/ notified bodies to drive support of the… more
- J&J Family of Companies (Spring House, PA)
- …and functional partners-including Translational Research, Precision Medicine, Regulatory Affairs , Market Access, and Clinical Development-to implement end-to-end ... data science solutions that drive scientific and operational impact. The successful candidate will lead matrixed teams, including technical data science groups (eg,… more
- City of New York (New York, NY)
- …essential cross-cutting support for non-clinical functions within the Office of Medical Affairs . You will gain broad exposure by assisting teams involved in critical ... areas like drug-resistant TB case management and regulatory affairs . This position requires a highly organized, detail-oriented, and flexible individual willing to… more
- Boehringer Ingelheim (Ridgefield, CT)
- …provides subject matter expertise to the US Clinical Development and Medical Affairs (CDMA) TA team, contributing to the strategic direction of evidence generation ... EPI&RWE strategy is developed as part of the Medical Affairs plan/ICP, and that the plan is executed throughout...a global and local level and assume a strategic scientific leadership position in US CDMA within the framework… more
- Sanofi Group (Cambridge, MA)
- …that is part of the Global Rare Disease Medical Team. Our Medical Affairs function serves as a key strategic partner with commercial, regulatory, clinical, HEVA ... needed + Lead the execution and support the strategy of global Medical Affairs studies, including the management of the study Steering Committee, development of the… more