- J&J Family of Companies (Spring House, PA)
- …future therapies. **What's in it for you:** If you have a creative scientific , translational and strategic mindset and you thrive on (1) identifying opportunities ... for (cross disciplinary) project impact, (2) raising the scientific bar of our discipline and (3) challenging/defending scientific and/or strategic project views… more
- Organon & Co. (Plymouth Meeting, PA)
- …modeling vendors) colleagues. The Clinical Pharmacology Lead will ensure the scientific and clinical pharmacology components of study protocols are sound, based ... colleagues in preclinical science, data science, clinical operations, regulatory affairs , chemistry, manufacturing and control (CMC), project management and other… more
- Merck (Upper Gwynedd, PA)
- …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects + ... company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. **The Clinical Director… more
- Merck (Harrisburg, PA)
- …field-based employees such as the Vaccine Key Customer Leader (VKCL), Vaccine Medical Affairs Leader (VMAL), Region Medical Director (RMD) as well as other members ... and health care environment knowledge through self-study of company-provided scientific , product and marketplace information, attendance at product workshops and… more
- Teva Pharmaceuticals (West Chester, PA)
- …responsibilities include statistical input to the evidence generation planning, medical affairs and RWE research proposal reviews, study protocol and statistical ... analysis plan (SAP) development and execution, results interpretation, scientific presentations and publications, interactions with agencies, and RWE/statistical… more
- Merck (North Wales, PA)
- …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. **The Senior Director is… more
- CSL Behring (King Of Prussia, PA)
- …therapeutic area/ project needs. **Main Responsibilities:** 1 Contribute to the scientific development of clinical programs and individual clinical studies in ... the clinical development plan within the assigned therapeutic area. 2 Provide scientific and clinical development input for the safe, efficient, and timely execution… more
- Merck (North Wales, PA)
- …Cross-Functional Teamwork, Drug Development, Global Strategy, Innovation, Regulatory Affairs Management, Regulatory Strategy Development, Regulatory Submissions, ... **Job Description** The Associate Director, Regulatory Affairs , supports products in the Oncology therapeutic area as part of a regulatory team. The individual will… more
- Sanofi Group (Swiftwater, PA)
- …Common Technical Document) prepared by the team to ensure appropriate quality and scientific content. + With the support of the Global Head of Vaccines clinical ... is the minimum education requirement. Advanced degree in a scientific related field is preferred. + 7+ years of...support of drug development, or equivalent experience in Regulatory Affairs or Medical Affairs . Knowledge of Vaccine… more
- Pfizer (Collegeville, PA)
- …role in regulatory policy priorities by representing Pfizer in appropriate scientific or regulatory activities (eg, membership in advisory councils and/or trade ... line help them achieve their full potential. **QUALIFICATIONS / SKILLS** + Advanced Scientific Degree (MD, Ph.D., PharmD) with a minimum of 10 years' experience in… more