- J&J Family of Companies (Skillman, NJ)
- Senior Associate , Regulatory Affairs - 2407025090W **Description** Kenvue is currently recruiting for: Senior Associate , Regulatory ... NJ **Travel %:** <10% **Pay: 84k- 152k** **What you will do** The Senior Associate , Regulatory Affairs is responsible for developing regulatory… more
- Merck (North Wales, PA)
- **Job Description** Reports to the Director/ Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for ... and approval of all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional… more
- Bristol Myers Squibb (Princeton, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . Position Summary : Reporting to the Senior Direc tor , US and Above Market Medical and Market Access C&E ... Lead , this role partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug...leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory , IT, Audit, Finance and HR to build and… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** ** Associate Director, Policy Advocacy** The Associate Director, Policy Advocacy serves as the senior expert in ... in advancing policy change in support of the company's business objectives. The Associate Director will proactively research and stay abreast of new strategies and… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director, Global Labeling Lead where you will be responsible for the ... and alignment of the labeling strategy and labeling content. Interface with Senior Management Cross-Functional Team (GLOC) + In alignment with TAU/MPD Labeling Lead,… more
- Taiho Oncology (Princeton, NJ)
- …such as clinical operations, data management, Pharmacovigilance Operations, Medical Writing and Regulatory Affairs is a plus. + CPM or CPIM certification ... Associate Director, Outsourcing & Vendor Management Pleasanton, CA,...negotiate MSA, SOW/WO, and Change Order. + Meets with senior functional leaders to align with their goals and… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The Associate Vice President (AVP) has primary responsibility for the planning and directing clinical research activities involving new or… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** ** Associate Director, Policy Strategy and Capabilities** The Associate Director, Policy Strategy and Capabilities ... team, reporting to the Executive Director, Policy Development & Strategy. The Associate Director will develop and maintain the strategic planning digital platform,… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Associate Director will be responsible for supporting the development and ... our team members are challenged and engaged with the broader matrix teams. The Associate Director will work with our Brand, Customer Experience, and Finance teams to… more
- Novo Nordisk (Plainsboro, NJ)
- …Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs , Data Management, Biostatistics, Non-clinical, Medical ... safety surveillance sub-function within the US East Coast Development Hub comprised of Senior Global Safety Leads, Global Safety Leads and Senior Global Safety… more