- GRAIL (Concord, NH)
- …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome ... position supports the US Regulatory team in preparing Investigational Device Exemptions (IDEs), IDE supplements, pre-submissions, Premarket Approvals (PMAs), annual… more
- Otsuka America Pharmaceutical Inc. (Concord, NH)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... + Ensure regulatory intelligence specialists have continued access to regulatory, clinical trial, and public domain information resources to identify relevant… more
- Fujifilm (Concord, NH)
- **Position Overview** The Associate Clinical Specialist independently provides customer support of Fujifilm's ES equipment in the Endoscopy department and/or ... catalog for assigned customers. It serves as the primary clinical resource for the Company and its sales team...required. This position reports directly to the Zone Sales Director or Regional Manager. **Company Overview** At FUJIFILM Healthcare… more
- ConvaTec (Lexington, MA)
- … Associate Director plays a key role to the success of Convatec's clinical trials. The Associate Director , Clinical Trials Management oversees the ... trial management experience in conducting and leading global medical device clinical trials, preferably with a sponsor company. + Solid understanding of… more
- Fujifilm (Concord, NH)
- …product manager, product/technical director ). + Minimum 8 years of medical device experience with strong clinical background. + Prior experience in ... global R&D, operations, regulatory, global marketing, infection control, other companies/ device manufacturers, etc.) + Build and maintain strong relationships with… more
