- 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
- J&J Family of Companies (West Chester, PA)
- Senior Director , DePuy Synthes, Medical Affairs , TECA - 2406191890W **Description** Johnson & Johnson MedTech is recruiting a ** Senior Director , ... potential. At Johnson & Johnson, we all belong. This Senior Director provides medical affairs ...cross-functional partners, including but not limited to R&D, Clinical Affairs , Regulatory Affairs , Health Economics… 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
- J&J Family of Companies (Spring House, PA)
- … Affairs organization, we are currently seeking an IT Senior Manager, Technical Product Manager, Regulatory Excellence. **RESPONSIBILITIES** : The ... IT Senior Manager, Technical Product Manager (TPM), Regulatory...health for humanity. Learn more at https://www.jnj.com/. The Global Regulatory Affairs business technology team is focused… 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
- Pfizer (Collegeville, PA)
- **ROLE SUMMARY** The Vaccines Operational Excellence Director role is an integral member of the Operational & Change Excellence Team. The Vaccines Operational ... Excellence Director leads the development and implementation of key assigned...category-led initiatives that have an impact on multiple Medical Affairs stakeholders and markets. They combine organizational, project management,… 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
- Merck (North Wales, PA)
- …within Global Medical and Value Capabilities (GMVC) in Global Medical and Scientific Affairs (GMSA) that reports directly to the Director , Medical Operations, ... regulatory guidelines and compliance requirements pertaining to Medical Affairs operations, and, preferably, experience in navigating regulatory challenges… 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
- 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
- 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 ... projects; and + Assist the Senior /Executive Director in ensuring that appropriate Corporate personnel are informed of the progress of studies of our competitors'… 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