- Merck & Co. (Upper Gwynedd, PA)
- … success together with risk mitigation measures.-Lead development and execution of global product and project regulatory strategy (ies) by ensuring ... robust assessment of global regulatory CMC requirements and critical evaluation of supporting documentation to confirm acceptability and identification of… more
- Merck & Co. (North Wales, PA)
- …role will focus on supporting HPV. Under the guidance of an Executive Director , within the Value and Implementation, Outcomes Research the incumbent has the ... following responsibilities:1.) development of the integrated evidence strategy to support HTA/ reimbursement/ NITAG evaluations; 2.) development of overall Real… more
- Merck & Co. (North Wales, PA)
- …barriers to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programsIn ... the guidance of a senior leader, an Associate Principal Scientist/Associate Director , has primary responsibility for planning/managing real world and economic… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThis position participates in the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will ... advanced leadership and technical skills as part of a global , cross-functional team. You will build and coach your...This includes the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) Proven ability to… more
- Eisai, Inc (Exton, PA)
- …Development groups as well as with Facilities, Quality Assurance, Quality Control, Regulatory , and CMC Program Management departments.The Associate Director of ... If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and building a… more
- Organon (Plymouth Meeting, PA)
- …efficient, agile manner. Provide Regulatory CMC and oversight in developing global Regulatory CMC strategies and executing submissions related to diverse ... Job Description The Position The Principal Scientist ( Director ) Regulatory CMC is responsible for...He/she must have a depth of experience in defining global regulatory CMC strategies, superb collaboration skills,… more
- Teva Pharmaceuticals (West Chester, PA)
- …Chester, PA Teva office How you'll spend your day Define and execute the global clinical operations strategy and oversee the staff responsible for managing and ... with. The opportunity We are seeking an experienced Sr. Director , GCO Therapeutic Area Head to lead the strategic...Therapeutic Area Head to lead the strategic and operational global execution of all clinical trials within the Neuroscience… more
- Organon & Co. (Plymouth Meeting, PA)
- …Independently interact with worldwide regulatory agencies and/or subsidiaries regarding global regulatory strategy /registration requirements for one or ... **Job Description** **The Position** The Associate Director , Global Regulatory Lead... Director will be responsible to: + Develop regulatory strategy for their assigned products, in… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …: Reporting to the Vice President, Global Medical Affairs, the Executive Director , CNS Strategy , Global Medical Affairs is a leadership position ... leads across functions, they will ensure a CNS portfolio Global Medical strategy is in place, including...Otsuka prominence in CNS space + Provides input into regulatory documents, including product labeling + Accountable for resourcing… more
- Pfizer (Collegeville, PA)
- The Global Access Strategy and Pricing (GASP) Precision Medicine & Lung Cancer Director role directly impacts the ability to achieve business objectives by ... Sigvotatug Vedotin and PDL1V. The objective for the franchise strategy is to advance the treatment of lung cancer...combination partners. This position will function with a 'One Global Access and Value' mindset and work in an… more
- J&J Family of Companies (Titusville, NJ)
- …for humanity. Learn more at https://www.jnj.com/. **Position Summary:** The **Associate Director ,** **Neuroscience Strategy Implementation** , is a member of ... employee engagement. The Associate Director reports to the Director , Neuroscience Strategy Implementation. **Key Responsibilities:** + _Process… more
- Merck (Upper Gwynedd, PA)
- … success together with risk mitigation measures. + Lead development and execution of global product and project regulatory strategy (ies) by ensuring robust ... assessment of global regulatory CMC requirements and critical evaluation of supporting documentation...development, communication, lifecycle management and review of the CMC Regulatory Strategy Document for assigned projects. +… more
- System One (Malvern, PA)
- …and post market activities comply with internal processes and global regulatory standards. + Develop the strategy and manage the creation, review, ... Job Title: Director of Regulatory and Medical Affairs...and Medical Affairs SOPs to ensure full compliance with global regulatory requirements. + Maintain current knowledge… more
- Sumitomo Pharma (Trenton, NJ)
- …. Job Overview The Director , Medical Strategy ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...of the Medical Affairs team reporting to the Senior Director , Medical Affairs Strategy . The job is… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …for those with CNS disorders, we are seeking a skilled and experienced Medical Director of CNS Early Assets, Global Medical Affairs, responsible for certain ... CNS TA which align to the broader overall TA strategy determined by the Sr. Director , Franchise... global value and real-world evidence, US and global commercial teams, market access, and regulatory … more
- J&J Family of Companies (Spring House, PA)
- …approved by the Company. **We are searching for the best talent for Associate Director , Regulatory Medical Writing - Oncology.** **Purpose:** + Able to function ... independently. + Leads in setting functional tactics/ strategy . + Leads project-level strategy (eg, submission team, global program team, clinical team). +… more
- Organon & Co. (Plymouth Meeting, PA)
- …**The Position** Leading the Regulatory Policy and Intelligence activities for Global Regulatory Affairs covering all Therapeutic Areas and products, as well ... or regions of the world of interest to Organon. **Responsibilities** + Provide Global Regulatory Policy and Intelligence insights to the organization to guide… more
- CBRE (Trenton, NJ)
- Business Development Senior Director , Global Occupier Accounts Job ID 210942 Posted 02-May-2025 Service line GWS Segment Role type Full-time Areas of Interest ... is Senior Managing Director , Business Development** The Senior Business Development Director , Global Occupier Accounts, will lead the Healthcare sector Named… more
- UGI Corporation (King Of Prussia, PA)
- Director - Global Risk Location: King Of Prussia, PA, US, 19406 Workplace Environment: Hybrid Company: UGI Corporation Requisition Number: 26323 UGI Corporation ... Credentialing * Referral Bonuses * Employee Discount Programs Position Summary: The Director , Global Risk has responsibilities for day-to-day management of the… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director , GCD is responsible for all ... develop the drug in accordance with a clinical and regulatory strategy . + Working with experts and...trial implementation and management. + Complete understanding of the global regulatory requirements. + Working knowledge of… more