- Merck & Co. (North Wales, PA)
- Job DescriptionReports 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
- Merck & Co. (North Wales, PA)
- …, GLOBAL REGULATORY CMC Biologics (R5)Under general supervision of an Executive Director / Senior Director , the Principal Scientist / Director is ... divestment and product withdrawal.Support new technology development.Demonstrate an understanding of regulatory affairs and applies this understanding to the… more
- Merck & Co. (North Wales, PA)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.-Specifically, the Director may...development projects; andAssist the Senior Director , Executive Director , and/or… more
- Merck & Co. (North Wales, PA)
- Job DescriptionUnder the guidance of a Senior Director , within Outcomes Research (OR) the incumbent has the following responsibilities: Development of the ... of patient reported outcomes, epidemiological studies and economic modeling.The Director also works closely with Product Development Teams, Franchise Teams,… more
- Merck & Co. (North Wales, PA)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Director May Be… more
- Merck & Co. (North Wales, PA)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... development projects; andAssist the Senior /Executive Director in ensuring that appropriate Corporate personnel are informed of the progress of studies of our… more
- CSL Behring (King Of Prussia, PA)
- The Senior Director , Head of Medical Affairs , LatAm & Partner Business will provide strategic, operational, and medical leadership for a high-performance ... Medical Affairs organization across the CSL Behring responsible cluster, supporting... cluster team to oversee and interact with relative regulatory agencies. *Functions as the scientific medical expert internally… more
- CSL Behring (King Of Prussia, PA)
- The Senior Director , Global Medical Affairs Pipeline Hematology is responsible for the development and execution of global medical affairs strategies ... international stakeholders. Serves as a collaborator and key stakeholder to the relevant senior leaders in Medical Affairs in the US and International, Global… more
- CSL Behring (King Of Prussia, PA)
- The Senior Director Medical Affairs Inline Bleeding will provide strategic medical leadership across all inline bleeding products. This is a critical role to ... as a collaborator and key stakeholder to the relevant senior leaders in Medical Affairs in the...personnel are trained and strong in medical, scientific, and regulatory knowledge as well as industry research and trends.… 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
- CVS Health (Harrisburg, PA)
- …perform a share of special clinical investigations and research as requested by the Senior Medical Director , Medical Affairs . These projects can include ... perform a share of special clinical investigations and research as requested by the Senior Medical Director , Medical Affairs . These projects can include… 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)
- …GLOBAL REGULATORY CMC Biologics (R5)** Under general supervision of an Executive Director / Senior Director , the Principal Scientist / Director is ... product withdrawal. + Support new technology development. + Demonstrate an understanding of regulatory affairs and applies this understanding to the benefit of… more
- Teva Pharmaceuticals (West Chester, PA)
- …key documents (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Senior Director will provide input ... and other global regulatory filings. **How you'll spend your day** The Senior Director will foster relationships with opinion leaders in assigned areas. +… 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
- Veterans Affairs, National Cemetery Administration (Philadelphia, PA)
- …advisor in the NAD office and provides advisory services to the NAD Executive Director , NAD Chief of Operations, NAD staff, Cemetery Directors and their staffs on ... Serves as the principal financial staff advisor to the North Atlantic District (NAD) Director . Informs the NCA Director of Budget and Planning on the status… more
- Merck (Upper Gwynedd, PA)
- …execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Clinical Director May Be Responsible For:** + Evaluating ... **Job Description** The ** Senior Clinical Director (Sr. Principal Scientist)**...closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage… more
- The Cigna Group (Philadelphia, PA)
- **Job Purpose/Description** The Legal Compliance Senior Director - Express Scripts Medicaid and Commercial is responsible for the development, implementation, ... across the organization to identify and mitigate compliance risks. The Legal Compliance Senior Director - Express Scripts Medicaid and Commercial will serve as… more
- Teva Pharmaceuticals (West Chester, PA)
- Senior Director , Patent Attorney - Small...to minimize IP risk + Collaborate with Legal and Regulatory Affairs to ensure effective Hatch-Waxman strategy ... a difference with. **The opportunity** We are seeking a dynamic and experienced ** Senior Director , Patent Attorney - Small Molecule** to develop and implement… more
- CSL Behring (King Of Prussia, PA)
- The Sr. Director , Head of Global Medical Information will oversee the global core functions of Medical Information across all therapeutic areas/products at CSL ... Clinical R&D, Pharmacovigilance, Quality, Marketing, Global Market Access/HCS, Heads of Medical Affairs in the US and International, TA Heads and global medical… more
