- Institute for Medical Research (Durham, NC)
- …research lab. Grants and Contracts Coordinator will report to the Proposal and Grant Writer Team Lead or designee. The successful candidate will have the ... Contracts Coordinator to assist with pre-award research planning for clinical research studies conducted by the Principal Investigator, Dr....under the direct supervisor of the Proposal and Grant Writer Team Lead . The prior statements describe… more
- J&J Family of Companies (Raleigh, NC)
- …practices across R&D. Principal Responsibilities: Leadership: + With a focus on clinical scientific content, lead early strategic submission discussions in ... The Director, Regulatory Medical Writing (RegMW) is a highly experienced medical writer and influential leader with strategic responsibilities as it relates to the… more
- IQVIA (Durham, NC)
- **Job Overview:** As a Lead Medical Writer on most types of writing projects. You will prepare assigned documents in accordance with IQVIA Standard Operating ... and to customers when appropriate. Keep abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along… more
- J&J Family of Companies (Raleigh, NC)
- …some mentorship from functional management and clinical team, as needed. + If a lead writer for a program: Be the primary point of contact and champion for ... Authoring experience with investigator brochures, clinical study protocols, and clinical study reports. Experience with common technical document summaries… more
- Takeda Pharmaceuticals (Raleigh, NC)
- …Regulatory Writing and Submission Support, _Oncology and Marketed Products_ . Team lead , based in Cambridge, MA/Virtual. Here, you will be a vital contributor ... such as Briefing Books (BB), Investigational New Drug Applications (INDs), Clinical Trial Applications (CTAs), Investigator's Brochures (IBs), New Drug Applications… more