- Merck (Rahway, NJ)
- …chance to see if we are the right company for your long-term goals Global Regulatory Affairs (GRA) Product Managers (PMs) are responsible for developing CMC ... preparation and review of information required for development of regulatory CMC dossiers for new and existing...organize LoQs + Analyze and trend; develop metrics + Regulatory Affairs Detailed Application Verification (DAV)- verification,… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …independently, as needed + Partners cross-functionally with departments such as Regulatory Affairs , Toxicology, CMC /Formulations, Biostatistics, Legal, ... strategy, working closely with other functional areas such as commercial, regulatory , pharmacovigilance, CMC , early clinical, and pre-clinical development in… more
- University of Maryland, Baltimore (Baltimore, MD)
- …in the MS in Regulatory Science program, with a focus on introductory and regulatory affairs aspects of the program, as well as another aspect of the program ... AREAS OF EXPERTISE AND EXPERIENCE_* Regulatory science, including introductory and regulatory affairs aspects, as well deep knowledge in another aspect (eg… more
- Merck (Rahway, NJ)
- …be able to work with all levels of management within and outside of Global Regulatory Affairs and Clinical Safety (GRACS). + Interact closely with the system ... differences **Preferred Experience and skills:** Five years' experience in Pharmacovigilance/ Regulatory / CMC /Quality/Clinical **NOTICE FOR INTERNAL APPLICANTS** In accordance… more
- IQVIA (Durham, NC)
- …rendered will adhere to applicable Johnson & Johnson SOPs, Wis, policies, local regulatory requirements, etc. + Co -author of the IPPI and review/provide input ... interface to ensure overall IPPI ad ministration adherence. The SIPS will be co -author of the IPPI, and will be responsible for training slide development, training… more