- Merck & Co. (North Wales, PA)
- Job DescriptionThe US Director of Medical Affairs (DMA) for Gynecologic Malignancies (Ovarian, Endometrial and Cervical Cancer) holds primary responsibility for ... the development and execution of regional oncology Medical Affairs strategies and plans for Gynecological Malignancies in the US across indications.- The US DMA for… more
- Merck & Co. (Upper Gwynedd, PA)
- …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... Management Process, Medical Research, Mentorship, Plan of Action and Milestones (POA&M), Regulatory Affairs Compliance, Regulatory Compliance {+ 5… more
- Larimar Therapeutics (Philadelphia, PA)
- …the day - we welcome you! Position Summary: Larimar is seeking a CMC Regulatory Affairs Director to provide professional experience and leadership supporting ... have significant expertise in discovery, non- clinical and clinical development, regulatory affairs , manufacturing...development through global marketing authorization approval and launch. The Regulatory Affairs Director will be… more
- Legend Biotech USA, Inc. (Philadelphia, PA)
- …commercial strategy.Collaborate closely with internal functions such as Pharmacology, CMC, Regulatory Affairs , Clinical , and Program Management.Maintain ... of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Sr. Director of Toxicology as part of the Clinical Development team based in… more
- Merck & Co. (North Wales, PA)
- …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... Neuropathic Pain, Neuroscience, Neuroscience Research, Pain Management, Pharmaceutical Development, Regulatory Affairs Compliance, Regulatory Compliance,… more
- Merck & Co. (North Wales, PA)
- …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director May Be Responsible For:Evaluating pre- clinical and translational… more
- Pfizer (Collegeville, PA)
- …and external partners, such as project leaders, research units, biostatistics, regulatory affairs , clinical pharmacology, human genetics, translational ... Experience working with and solid understanding of related disciplines, eg, Clinical Operations, Data Management, Safety, Biostatistics, Regulatory , Study… more
- Merck & Co. (North Wales, PA)
- …adherence, and outcomes while maintaining compliance with the highest ethical and regulatory standards.- The Director will collaborate closely with the US ... Job Description Director Global Marketing Immunology - IBD Patient Strategy...with Global Pharmaceuticals policy and Global Medical and Scientific affairs in support of IBD launchIdentify key elements of… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Regulatory Affairs Date: Dec 2, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: ... to make a difference with. **The opportunity** The Associate Director , Global Regulatory Affairs , will...cross-functional colleagues as well as members of the global regulatory team. * Critically reviews clinical and… more
- Sumitomo Pharma (Harrisburg, PA)
- …a dynamic, highly motivated, and experienced individual for the position of **Associate Director , Regulatory Affairs (Oncology).** The Associate Director ... is part of the Global Regulatory Affairs (GRA) team based in the US. He/She will...to electronic regulatory submissions and working with regulatory templates + Understanding of EU Clinical … more
