- Merck (North Wales, PA)
- …process including the related SOPs and Execution resources. The incumbent is accountable to Sr . Director of Business Process and Systems with input from VP, CSRM ... external stakeholders, contributing functional areas and process governance committees. Works with Sr . Director for Business Process and Systems, CSRM to develop… 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 ... 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
- CSL Behring (King Of Prussia, PA)
- …will also partner with teams from Global Commercial Development, Clinical Research and Regulatory Affairs to ensure North America is represented on all future ... **CSL Behring is seeking a Sr . Director , New Product Planning &...multiple teams and people including marketing leadership, US Medical affairs , US Health Care Systems teams, global partners, and… 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
- Merck (North Wales, PA)
- …placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be responsible for:** + Providing scientific ... with talented and dedicated colleagues while developing and expanding your career. The Senior Clinical Director ( Sr . Principal Scientist) has primary… 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)
- …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)
- …with talented and dedicated colleagues while developing and expanding your career. The Senior Director ( Sr . Principal Scientist) has primary responsibility ... placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director may be responsible for: + Evaluating pre-clinical… 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
- 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