- Teva Pharmaceuticals (West Chester, PA)
- Senior Director Regulatory Affairs CMC (Biologic Products) Date: May 15, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva ... and new people to make a difference with. **The opportunity** The Sr. Director , Global Regulatory Affairs CMC is responsible to oversee and help develop … more
- Teva Pharmaceuticals (West Chester, PA)
- Senior Director , Regulatory Affairs II Date: May 19, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job ... a difference, and new people to make a difference with. **The opportunity** The Senior Director , Regulatory Affairs II will have a knowledge of global… more
- CSL Behring (King Of Prussia, PA)
- …biotherapies used to treat serious and often rare conditions. Could you be our next Senior Manager of Regional Regulatory Affairs ? This position is located ... is a Hybrid role. You will report to the Director , Regional Regulatory TA Lead. **RESPONSIBILITIES:** +...GRA NA representative for assigned projects to the Global Regulatory Affairs Strategy Team (GRAST) to provide… more
- Pfizer (Collegeville, PA)
- …and integrate these insights to co-create and lead a global medical strategy. The Senior Director will: + Be accountable for the development and execution of ... benefit from our current and future medicines. The Global Senior Medical Director - Abrocitinib Team Lead...Director will develop and execute a comprehensive Medical Affairs strategy for Abrocitinib. He/She needs to show a… more
- Pfizer (Collegeville, PA)
- …vaccines. **What You Will Achieve** You will represent Pfizer as anApprovalLiaison in the regulatory affairs team. You will play the critical role of providing ... strategic regulatory expertise as Global regulatory representative to Product Team(s). As a Director...Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States. Regulatory Affairs… more
- Merck (North Wales, PA)
- **Job Description** Under general supervision of an Executive Director / Senior Director , the Principal Scientist / Director is responsible for developing ... product withdrawal. + Support new technology development. + Demonstrate an understanding of regulatory affairs and applies this understanding to the benefit of… 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 (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
- J&J Family of Companies (Spring House, PA)
- …quality monitoring & compliance, data management, global medical safety, biostatistics, regulatory affairs , clinical supplies unit, medical writing, clinical ... Director , Project Responsible Physician - Neuroscience - 2406186566W...Committee (IDMC) and adjudication meetings as needed. + Assists Regulatory Affairs in determining requirements for any… more
- Organon & Co. (Plymouth Meeting, PA)
- …stakeholders, including Medical Affairs , Sales, Marketing, HCP Engagement, Compliance and Regulatory . The role will report to the Director , US Medical ... collaboration skills, including cross-divisionally with colleagues from Sales, Medical Affairs /Clinical, Compliance/Quality, and Regulatory . + Experience working… more
- CSL Behring (King Of Prussia, PA)
- The Associate Director of US Market Access - New Products will lead US value, access, pricing, and reimbursement strategy in preparation for the launch of several ... access strategy, reimbursement planning, and early account engagement. This Associate Director is responsible for developing and executing the market access… more
- J&J Family of Companies (Malvern, PA)
- …Development, Therapeutic Area Teams, Health Policy and Advocacy, Communications, Scientific Affairs , R&D, Senior Leadership) + Monitor the stakeholder ... Director , Patient Advocacy, R&D (1 of 2) -...bioethics, legal, policy, and compliance. Externally, with patient organizations, regulatory bodies and other external stakeholders. This is a… more
- Merck (North Wales, PA)
- …colleagues, GCTO Country Operations, other GCTO functional areas, Pharmacovigilance (PV), Global Regulatory Affairs and Clinical Safety (GRACS), IT, etc.) is ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing… more
- Pfizer (Collegeville, PA)
- **ROLE SUMMARY** The Director , Commercial Effectiveness Cardiovascular Lead is a key partner to the Cardiovascular Sales team leadership. They work to maximize the ... brand commercial leads, sales, account management, payer, Medical, corporate affairs , legal, finance, external third-party vendors, operations and Digital. Key… 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 (Sr. Principal Scientist) has primary responsibility for the… more
- Endo International (Malvern, PA)
- …for talented individuals to join our team. **Job Description Summary** The Senior Medical Information Manager has the primary responsibility to support Medical ... Committees. + Work closely with Research and Development, Clinical Operations, Regulatory , and Legal to coordinate development, approval, and communications of all… 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
- Pfizer (Collegeville, PA)
- …across the Commercial business. We are looking for an individual contributor ** Director Analytics Data Architect** , that will serve as an experienced and ... The scope of responsibility spans drug discovery and development, medical affairs , marketing and brand management, sales, managed markets, manufacturing operations,… more