- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- AbbVie (North Chicago, IL)
- …of an overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's ... generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy. Responsibilities: + Manages the design and… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced knowledge of regulatory ... you and empower you to shine? Join us as Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge,...a MIDD path within each project. + Leads strategic, scientific , and operational aspects of multiple drug development projects… more
- Pfizer (Olympia, WA)
- **ROLE SUMMARY** The Internal Medicine Field Medical, Director is responsible for providing Migraine therapeutic area/product expertise for the designated ... with Pfizer as appropriate + Understand the priorities of Pfizer Medical Affairs in order to contribute to Medical educational content strategy development and… more
- Amgen (Washington, DC)
- …research opportunities. + Provide clinical content input to materials to be used in Scientific Affairs as well as the Commercial Organization + Approximate 10% ... + Support cross-functional and global collaborations to integrate broad medical, regulatory , safety, scientific , and commercial access and value input… more
- Otsuka America Pharmaceutical Inc. (Santa Fe, NM)
- …including INDs, IBs, clinical study reports, and NDAs/BLAs. + Collaborate with regulatory affairs on interactions with global health authorities. + Provides ... with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director , GCD...programs after proof of concept through late-stage trials and regulatory submissions. + Provide medical and scientific … more
- J&J Family of Companies (Titusville, NJ)
- …Organization, Finance and Procurement, Global Commercial Strategic Organization, Global Medical Affairs , Regulatory Affairs , Research & Development, Global ... CAPLYTA(R) medical team to support our growing impact in psychiatry. The Director , Program Management (PM) is primarily responsible for leading the program… more
- Abbott (Pleasanton, CA)
- …have an exciting opportunity for a seasoned leader to join our Global Clinical and Regulatory Affairs team within the Heart Failure Division (HFD) as the Global ... and resources) by working closely with internal stakeholders (R&D, Marketing, Clinical Affairs , Regulatory Affairs , Medical Affairs , Reimbursement)… more
- Boehringer Ingelheim (Ridgefield, CT)
- …field with eight to ten (8-10) years' experience in the pharmaceutical industry in Regulatory Affairs or scientific discipline required OR Master's degree ... Boehringer Ingelheim's high regard for our employees. The Associate Director , DRA Product Labeling will lead and manage the...six (6) years' experience in the pharmaceutical industry in Regulatory Affairs or scientific discipline… more
- Bristol Myers Squibb (Princeton, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary:** The Director for Admilparant will provide deep disease state knowledge in ... strategy, planning, development, and implementation of the US/Global medical plan. The Director will report to the Senior Director , Admilparant Medical Program… more