- J&J Family of Companies (Titusville, NJ)
- …Clinical Development & Research - Non-MD **Job Category:** Scientific /Technology **All Job Posting Locations:** Allschwil, Switzerland, Beerse, Antwerp, ... interactions includes individuals from TA strategy, GCSO, global regulatory affairs , project management, finance, legal, quality assurance, quality monitoring &… more
- Teva Pharmaceuticals (Los Angeles, CA)
- …compliant relationships with peers leading teams in Marketing, Market Access, Patient Services, and Medical Affairs . + Work in concert with the Field Sales team ... Director , Marketing - Thought Leader Liaisons CNS- Remote...and specific product and therapeutic area goals. + Leverage scientific insights and strategic relationships to drive Teva's commercial… more
- Takeda Pharmaceuticals (Boston, MA)
- …of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, ... my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for...**What you bring to Takeda:** + BSc in a scientific or allied health/ medical field (or equivalent… more
- Takeda Pharmaceuticals (Boston, MA)
- …of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, ... Quality program leadership team. **What you bring to Takeda:** + BSc in a scientific or allied health/ medical field (or equivalent degree). + Minimum of 7… more
- J&J Family of Companies (Titusville, NJ)
- …**Job Description:** Johnson & Johnson Innovative Medicine is recruiting for a Director , R&D Data Science & Digital Health - Hematology, Oncology. This position ... partners (eg, Translational research, Precision Medicine and diagnostics, Regulatory Affairs , Market Access, Clinical Development) to identify and implement… more
- HRPivot (Tucson, AZ)
- …proven R&D leader to drive the development of a highly advanced Class III medical devices through concept, preclinical, and clinical stages to FDA PMA approval. The ... leadership role shaping next-generation life-sustaining technologies. Position Summary: The Director of Research & Development will lead the design, development,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …indicators, training, and scope/remit. + Successfully partner with Global Commercial, Medical Affairs , Business Conduct, Finance, Regulatory, and other cross ... team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve… more
- AbbVie (South San Francisco, CA)
- …physicians, epidemiologists, safety analysts), Statistical Programming, Clinical Statistics, Regulatory Affairs , and Medical Writing. Safety Statisticians work ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Oncology TA Head in our Safety Statistics team. The Director will have oversight of statisticians in oncology. This… more
- Otsuka America Pharmaceutical Inc. (Juneau, AK)
- …answer questions from HTA agencies. + Ensure global and regional value evidence, medical , market access and government affairs teams are working seamlessly to ... **Position Summary:** The Director , Health Technology Assessment (HTA) Lead, is responsible...HTA submissions. + Experience in conducting HEOR studies. + Scientific expertise in HTA/ HEOR. + Experience in developing… more
- AbbVie (Barceloneta, PR)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The ME&C Associate Director is a global program management expert responsible for managing major… more