- 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 ... 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
- Takeda Pharmaceuticals (Exton, PA)
- …of proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance, execute and ... my knowledge. **Job Description** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
- Takeda Pharmaceuticals (Exton, PA)
- …potential issues. POSITION ACCOUNTABILITIES: + Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance organizations ... **Job Description** About the role: Join Takeda as a Senior Manager, US Medical Ad/Promo Regulatory Review... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
- Merck (North Wales, PA)
- …placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be responsible for:** + Providing scientific ... medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of clinical development,… more
- Merck (North Wales, PA)
- …Description** **Position Description:** **Associate Director , Policy Advocacy** The Associate Director , Policy Advocacy serves as the senior expert in the ... policy change in support of the company's business objectives. The Associate Director will proactively research and stay abreast of new strategies and tactics… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** ** Director , Policy Development** The Director , Policy Development serves as the leading expert on above-product ... and geo-political changes that will impact our global business. The Director independently and proactively identifies risks and opportunities, conducts analysis (or… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** **Associate Director , Policy Strategy and Capabilities** The Associate Director , Policy Strategy and Capabilities ... across the Strategic Planning & External Engagement team, reporting to the Executive Director , Policy Development & Strategy. The Associate Director will develop… more
- Teva Pharmaceuticals (West Chester, PA)
- …have a significant impact on drug development programs and have visibility with senior level management. A Director , Clinical Statistics may be an individual ... Director , Clinical Statistics Date: Sep 19, 2024 Location:...significant experience in drug development and clinical research, including regulatory interactions both inside and outside of the US.… more
- Merck (Upper Gwynedd, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... projects; and assist the Senior /Executive Clinical Director /Vice-President in ensuring that appropriate corporate personnel is informed of the progress of… more
- Merck (North Wales, PA)
- …monitoring, analysis, regulatory reporting, and publication. **Specifically, The Senior Director May Be Responsible For** + Evaluating pre-clinical ... talented and dedicated colleagues while developing and expanding your career. The Senior Director ( Senior Principal Scientist) has primary responsibility… more
- J&J Family of Companies (West Chester, PA)
- …case-by-case basis and if approved by the Company. The position reports to a Senior Director of MedTech Epidemiology & Real-World Data Sciences within the ... Senior Analyst, Epidemiology and Real-World Data Sciences -...globally, 2) evaluations of product safety, 3) evidence for regulatory approvals (pre- and post-approval), 4) advancing the use… 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 ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director may… more
- Merck (North Wales, PA)
- …have managerial responsibilities of ADT Leaders or Team Members that could include Executive Director , Senior Director , or Director level personnel ... + Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development… more
- CSL Behring (King Of Prussia, PA)
- …manufacture and commercial launch. Interface with other disciplines including Global Regulatory Affairs , Project Management, Operations and Commercial Operations ... 3 sentences). The purpose of the position of Executive Director R&D Quality is to lead a dedicated team...is responsible for the leadership and co-ordination of all regulatory GxP inspections for the R&D teams and across… more