- J&J Family of Companies (Spring House, PA)
- Director , Regulatory Medical Writing (1 of 4) - 2406211847W **Description** Johnson & Johnson is currently seeking a Director , Regulatory ... people can reach their potential. At Johnson & Johnson, we all belong. The Director , Regulatory Medical Writing (RegMW) is a highly experienced … more
- J&J Family of Companies (Spring House, PA)
- Associate Director , CMC Regulatory Affairs - 2406221330W **Description** Johnson & Johnson is recruiting for an Associate Director , CMC Regulatory ... Authorities. + Provides technical expertise and technical input in the preparation and writing (as applicable) of regulatory dossiers for submission to Health… more
- Organon & Co. (Plymouth Meeting, PA)
- …support the approved early development plans. The TMED Lead will serve as the medical monitor and/or study director responsible for the execution (in conjunction ... **The** **Position** **This position can be 100% remote in the US** The Director , Translational Medicine and Early Development (TMED) Lead will be responsible for… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …**__** Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can ... other than @Olympus.com, it is likely not legitimate._ **Job Description** The Director Scientific Communications, Global Operations plays a central role in the… more
- Merck (North Wales, PA)
- …lead clinical scientist on the clinical trial team. + Collaborates with the Medical Writer on clinical/scientific and regulatory documents. + Partners with Study ... of clinical data/ medical protocol deviations in collaboration with the Clinical Director . + Builds talent and capabilities of direct and indirect team members… more
- Organon & Co. (Plymouth Meeting, PA)
- …promotional regulatory strategy in collaboration with Commercial, PRT, Global Regulatory Liaisons, Medical Affairs and Worldwide Product Labeling. + Guide ... writing ability, effective communication and familiarity with worldwide regulatory agencies. + Experienced in negotiations with health authorities. + Outstanding… more
- J&J Family of Companies (Spring House, PA)
- …such as nonclinical safety, pharmacokinetic, and discovery biology project leaders, medical writers, global regulatory dossier leaders, and other subject ... Skills:** **Required:** + Experience working globally as lead author on writing Toxicology, Pharmacology, Pharmacokinetics, or Bioanalytical regulatory documents… more
- Pfizer (Collegeville, PA)
- …study team in governance meetings and submissions, partners with/supports the Development lead/ Medical Director regarding study and disease area strategy. + ... **ROLE SUMMARY** The Late-Stage Clinical Scientist (non-MD, Director ) is responsible for scientific oversight, data integrity and quality of clinical trial(s) in… more
- CSL Behring (King Of Prussia, PA)
- …drug development and manufacturing processes for pharmaceuticals (CMC, non-clinical, clinical, Regulatory Affairs). **BENEFITS** + Medical , Dental Vision + 401K ... around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines...or Bern Switzerland office. You will report to the Director of Global Clinical Science Lead. **Responsibilities:** + You… more