- Bristol Myers Squibb (Princeton, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** The ... + Prepare content for regulatory strategic documentation and Regulatory Project Reviews. Align regulatory plans with commercial and development plans… more
- AbbVie (Florham Park, NJ)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Director , Statistics provides scientific and statitical leadership for assigned ... clinical development projects. A visible and collaborative role, the...or those of a team. Lead/develop statistical strategy for project development and regulatory submission. + Direct or provide… more
- Bristol Myers Squibb (Madison, NJ)
- …levels of the organization. + Knowledge of overall project planning and project management of clinical trials. + Proven ability to partner effectively with ... personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Oncology & Hematology - will: + Support relationships with… more
- Bristol Myers Squibb (Princeton, NJ)
- …**Position Summary** As a key member of the Congress Excellence Team, the Associate Director , Congress Engagement will play a pivotal role in shaping and guiding the ... educational activities, and pre- and post-congress deliverables. The Associate Director , Congress Engagement is responsible for championing effective execution… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Principal Medical Writer Associate Director **Location** : USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for ... started? **Main Responsibilities:** **Document Development** + Create high-quality regulatory-compliant clinical documents supporting product life cycle + Ensure timely… more
- Bristol Myers Squibb (Princeton, NJ)
- …and PK (pharmacokinetics) support for all pipeline assets throughout clinical development, from candidate nomination through registration and lifecycle management. ... drug-interaction potential of drug candidates. Working closely with drug safety and clinical pharmacology, Development DMPK plays a critical role in IND submissions… more
- Bristol Myers Squibb (Princeton, NJ)
- …or market access objectives in a global organization. The Senior Director provides expertise and guidance in collaboration with cross-functional groups broadly ... with regards to planning, execution, interpretation and regulatory submission of clinical projects and studies. Provides guidance and management to statisticians to… more
- Merck (Rahway, NJ)
- …pipeline programs using fed-batch and continuous manufacturing platforms. The Director , Biologics Process Development (BPD) within the Biologics Process Research ... with superior product quality and allow speedy progression for clinical studies and commercial launch. The candidate will be...or downstream areas) or manufacturing is required; ability to project achievable project plans to ensure effective… more
- Terumo Medical Corporation (Somerset, NJ)
- Sr. Director , HR Strategy Date: Aug 9, 2025 Req ID: 4847 Location: Somerset, NJ, US, 08873 Company: Terumo Medical Corporation Department: TMC Human Resources Terumo ... products, training and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is part… more
- RWJBarnabas Health (Oceanport, NJ)
- Director , Revenue Cycle Automation and OptimizationReq #:0000202284 Category:Leadership Status:Full-Time Shift:Day Facility:RWJBarnabas Health Corporate Services ... per year Location: 2 Crescent Place, Oceanport, NJ 07757 Job Title: Director Location: Barnabas Health Corp Department: Patient Accounts Req#: 0000202284 Status:… more