- ThermoFisher Scientific (Mount Prospect, IL)
- …analysis tools (eg, 6M, Fishbone, TapRooT) and general problem-solving techniques. + Lead , initiate, and assist with the completion of immediate corrections and CAPA ... industry. + Minimum of 3 years of experience in technical or scientific writing principles. + Demonstrable knowledge of...to mentor and train others. + Experience with training technical writing skills and Root Cause Analysis Tools preferred.… more
- Suny Polytechnic Institute (Utica, NY)
- …and editing of figures and other graphical elements. Work may include being the lead writer on non- technical applications. + Identify resources both internal ... Professional Posted On: Tue Jul 23 2024 Job Description: The Grant Writer will identify funding opportunities, draft proposals, prepare supporting documentation and… more
- Pfizer (Pearl River, NY)
- **Role Summary** The Global Clinical Lead functions independently and has direct experience with all the steps in designing and delivering results of clinical ... by applying extensive expertise and in-depth knowledge of clinical research to lead global clinical research programs and registration activities across one or more… more
- University of Southern California (Los Angeles, CA)
- …This position entails providing support for the USC NCCC IITs as a scientific writer and editor as well as working within the interdisciplinary clinical trials teams ... to stay current on policy and guidelines to ensure high quality Investigator Initiated clinical trials managed by the Clinical Investigations Support Office (CISO).… more
- 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 ... planning for clinical research studies conducted by the Principal Investigator , Dr. Stephen Freedland, and his associates in his...under the direct supervisor of the Proposal and Grant Writer Team Lead . The prior statements describe… more
- J&J Family of Companies (Columbus, OH)
- …with 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 ... documents such as, but not limited to, clinical study reports, investigator 's brochures, study protocols, summary documents, risk management plans, regulatory… 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 ... to customers when appropriate. Keep abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with… more
- Takeda Pharmaceuticals (Columbus, OH)
- …Regulatory Writing and Submission Support, _Oncology and Marketed Products_ . Team lead , based in Cambridge, MA/Virtual. Here, you will be a vital contributor ... Investigational New Drug Applications (INDs), Clinical Trial Applications (CTAs), Investigator 's Brochures (IBs), New Drug Applications (NDAs), Biologic License… more