- City of New York (New York, NY)
- …teams involved in critical areas like drug-resistant TB case management and regulatory affairs . This position requires a highly organized, detail-oriented, and ... and manage correspondence; take clear and concise meeting minutes. - Assist the Regulatory Affairs Coordinator: Support the preparation and review of … more
- Genentech (South San Francisco, CA)
- …Team, alongside other senior leaders such as the VP, Head of Scientific Operations. This individual will manage a team of two Medical Science Health Population ... environments impacting Roche/Genentech, coupled with thorough knowledge of US regulatory /FDA requirements. + Scientific credibility and enterprise thinking… more
- Bristol Myers Squibb (Cambridge, MA)
- …Leadership organization are strategic-thinking, problem-solving, and action oriented scientific leaders who bring drug development and commercialization insights ... late-stage challenges (eg, trends in disease area therapeutic advances, and evolving regulatory , patient advocacy and market access environments) to create a vision… more
- Lilly (Indianapolis, IN)
- …teams, including medicinal chemistry/genetic medicines/bioproducts, toxicology/ADME, bioinformatics, and regulatory affairs , to integrate data and drive ... a track record of delivering impactful medicines that improve people's lives. ** Scientific and research leadership** + Provide strategic vision and direction for… more
- Lilly (Indianapolis, IN)
- …or experience in drug discovery or development, eg epidemiology, toxicology, pharmacovigilance, regulatory affairs . OR (BS Degree or equivalent experience in ... or experience in drug discovery or development, eg epidemiology, toxicology, pharmacovigilance, regulatory affairs . + Experience in drug development process. +… more
- Bristol Myers Squibb (Princeton, NJ)
- …decks, and review scientific content and publication + Collaborates with the Senior Director and medical matrix in the development of Customer Impact Plan and ... of the US/Global medical plan. The Director will report to the Senior Director, Admilparant Medical Program Lead. **Key Responsibilities:** + Support the execution… more
- System One (Park Ridge, NJ)
- …+ Partner with product development, packaging, operations, quality, and regulatory affairs to integrate microbiological and sterilization requirements ... technical direction, leading high-impact sterilization programs, and ensuring full regulatory compliance across the product lifecycle-from development through commercialization.… more
- J&J Family of Companies (Titusville, NJ)
- …health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Medical Writing **Job Category:** People ... will be considered as a single submission. **Purpose:** The Director of Regulatory Medical Writing (RegMW) is recognized as a leader with extensive medical… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …with cross-functional teams such as Marketing, Operations, Finance, Regulatory Affairs , Quality Assurance, Medical & Scientific Affairs , Legal, ... or franchises through strong collaboration with sales, marketing, operations, finance, regulatory affairs , quality assurance, medical/ scientific affairs… more
- Merck (Upper Gwynedd, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May Be… more