- Boehringer Ingelheim (Ridgefield, CT)
- …motivate others. + Experience managing and directing teams/vendors in process research /development, drug product formulations and clinical GMP CTM manufacturing. ... will be responsible for leading all DP-related activities within the project (s), in support of CMC development within EACD. The Associate Director/Senior… more
- State of Massachusetts (Boston, MA)
- …promulgating regulations. * Provide written and oral advice to the Agency on regulatory matters related to MSAC. * Establish and maintain strong relationships with ... MSAC Commissioners. * Introduce policy, regulatory , administrative, and enforcement issues for board consideration. *...inspections, and complaint investigation. * Should have strong planning, research , and organizational skills, and be able to … more
- Bassett Healthcare (Cooperstown, NY)
- …practice by employing educational strategies to promote positive learning and clinical competency in the practice environment. This is accomplished by assessment ... learning needs of the nursing staff and for promoting high quality clinical performance to enhance patient outcomes. + Utilizes creative and innovative strategies… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Associates, Clinical Data Managers and other Clinical , Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and ... colleagues to ensure appropriate design, statistical analysis and reporting of Gilead clinical data in efficiently achieving regulatory , scientific and business… more
- Abbott (San Diego, CA)
- …project deadlines. + Support and provide HFE expertise in preparation for clinical studies and regulatory submissions in accordance with HF standard ... external usability design resources, and reports progress on various project activities. **What You'll Work On:** + Act as...+ Act as a thought leader in domain of research , while advocating for people who use our products… more
- Novo Nordisk (Boulder, CO)
- …Watertown, Cambridge and Seattle reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for ... About the Department Our Research & Development organization brings together the best...such as Quality Assurance/ Control, Chemical Development, Program Management, Regulatory , Analytical Development, Materials Management, and Clinical … more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …Medical and Clinical development teams. + Oversee the US Investigator-Sponsored Research (ISR) and Collaborative Research (CR) program within the evidence ... Collaboration and Compliance** + Partner across Kite Medical Affairs, Clinical Development, Translational Medicine, Regulatory Affairs, and Product… more
- Merck (Albany, NY)
- …the team delivers high-impact scientific exchange, insights, congress engagement, and research contributions that advance US Medical Affairs (USMA) and Value and ... and timelines aligned to: Scientific Exchange, Insights, Scientific Congresses and Research . + Champions the team's contribution to USMA and V&I priorities;… more
- Taiho Oncology (Princeton, NJ)
- …while maintaining quality and advocating compliance. + Strong understanding of clinical development, post-marketing safety, and regulatory submissions. + Plan, ... or PharmD degree. + Extensive knowledge of the pharmaceutical research and development process and the regulatory ...TrackWise system is a plus. Demonstrated leadership skills. + Project and regulatory management abilities. + Excellence… more
- Seattle Children's (Seattle, WA)
- …two ongoing clinical trials treating patients with CAR T cells. The project will implement tumor triggered regulatory circuits to protect the engineered ... patients with cancer. The lab has a preclinical and clinical arm. The post-doctoral associate will be part of...Ben Towne Center for Childhood Cancer and Blood Disorders Research at the Seattle Children's Research Institution.… more