- Boehringer Ingelheim (Ridgefield, CT)
- …development, usually at Start of Development through phase I-III. The Senior Clinical Program Leader provides medical/ scientific , technical, and managerial ... **Description** The Senior Clinical Program Leader assumes global Clinical Development...studies to be conducted, and provides input to Medical Affairs strategy documents such as Scientific Platform,… more
- Abbott (Alameda, CA)
- …meets regulatory needs - Effectively interacts with project leaders, and regulatory affairs . - Responsible for the accuracy and appropriateness of ... - Demonstrates extensive understanding of statistical concepts and methodologies SCIENTIFIC REPORTS AND PUBLICATIONS - Responsible for Statistical Methods section… more
- Genentech (South San Francisco, CA)
- …highly experienced R&D attorney for life sciences/biotech clients, with deep experience in regulatory law related to early and late stage research and development of ... and medical devices. As a member of the R&D Law Group, this **" Senior Counsel Specialist, Assistant General Counsel"** role will primarily support Research and Early… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …with robust commercial insights and scenario planning. + Collaborate with R&D, Medical Affairs , Market Access, and Regulatory to guide evidence generation and ... Senior Director Global Product Strategy - Neuroscience Pipeline...product strategy for Teva's early-stage neurology pipeline - translating scientific innovation into long-term brand and business value. This… more
- Flywheel Partners (New York, NY)
- …Collaborate with a multi-functional account team to develop innovative medical and scientific educational materials tailored to our clients' needs. The audiences for ... pharmaceutical sales forces, account managers, clinical educators, and medical affairs . + Writing/Content Development + Research, learn, and simplify complex… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Olympus: https://www.olympusamerica.com/careers . **Job Description** As part of the Medical and Scientific Affairs group, an integral delivery unit within the ... Global Clinical Affairs organization, the Sr. Clinical Data Manager is accountable...and completeness of clinical trial data in compliance with regulatory standards, SOPs, and Good Clinical Data Management Practices… more
- Takeda Pharmaceuticals (Lexington, MA)
- …colleagues from Research, Quality Control, Process Development, Drug Product Development, and Regulatory Affairs to drive alignment on potency strategy and ... functions, guiding team members to successful execution. + Author technical reports, regulatory filing sections, and scientific publications as appropriate. +… more
- Conagra Brands (Chicago, IL)
- …internal departments and functions including Quality, Engineering, Thermal Processing, Sanitation, Scientific and Regulatory Affairs , Consumer Affairs ... As the Senior Microbiologist, reporting to the Microbiology Manager, you...FDA, and USDA standards; provide technical support to maintain regulatory compliance. + Collaborate outside of FSQRA organization to… more
- AbbVie (North Chicago, IL)
- …areas of work may include clinical trials, patient safety, and global medical affairs . Senior Managers works independently in partnership with experts in ... methodologies and innovations in drug development spanning trial design, monitoring and regulatory submissions, as well as post-marketing access. As a Senior … more
- Gilead Sciences, Inc. (Foster City, CA)
- …stakeholders to establish strong working relationships with quality groups, colleagues in Regulatory Affairs , Global Trade Ops, Global Commercial Operations & ... critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as...compliance across the US, Canada & LATAM regions. The Senior Director, Quality Assurance - Distribution will sit on… more