- ThermoFisher Scientific (Wilmington, NC)
- **Work Schedule** Standard Office Hours (40/wk) **Environmental Conditions** Office **Job Description** ** Senior ** ** Regulatory ** ** Medical Writer (FSP** ... location in the US. We are looking for a Senior Medical Writer to be...the use of software for document development, document types, regulatory requirements, and therapeutic area knowledge. + Ensures compliance… more
- Merck (Jackson, MS)
- …support the clinical regulatory writing portfolio. **With minimal oversight, the Senior Medical Writer :** + Demonstrates independence in preparing ... **Job Description** The Senior Medical Writer is...regulatory requirements. + Applies an in-depth knowledge of medical writing responsibilities, including document planning and authoring, and… more
- Bausch Health (Bridgewater, NJ)
- …creates it-where your skills and values drive our collective progress and impact. The Senior Medical Writer will have oversight of internal and external ... + Works with project teams to prepare clinical and regulatory documents, including protocols, study reports, investigator brochures, INDs/IMPDs,...+ At least 5 years of xperience as a medical writer or equivalent, or presenting relevant… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Senior Scientific Writer contributes to faculty success by collaborating with scientific and clinical teams to coordinate, develop, ... clinical study protocols, executive summaries, and strategic and progress reports. The Senior Scientific Writer also provides project management, mentors junior… more
- AbbVie (Mettawa, IL)
- …. Job Description *Employee can work remotely anywhere in the US The Senior Medical Writer is responsible for providing medical ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...required or in a related area such as quality, regulatory , publications, clinical research, or product support/R&D. 3 years… more
- University of Miami (Miami, FL)
- …- Protocol Development Office (PDO) has an exciting opportunity for a Full Time Scientific Writer ( Medical Writer ) to work Remotely. CORE JOB SUMMARY The ... Scientific Writer analyzes scientific data and translates complex scientific concepts,...5.Communicates (telephone, email, meetings) with principal investigator and key senior leadership authors as necessary to ensure the accuracy… more
- Stony Brook University (East Setauket, NY)
- Digital Content Writer **Position Summary** As a Digital Content Writer , you will play a crucial role in crafting engaging and informative content that connects ... copy for digital service line landing pages and campaigns. The Digital Content Writer reports to the Director Digital Marketing for Stony Brook Medicine. **Duties of… more
- Holtec International (Covert, MI)
- …and historic undertaking for the industry and the nation! JOB SUMMARY The Exam Writer develops and administers Regulatory Exams in accordance with NUREG 1021, ... Exam Writer Holtec Decommissioning International (HDI) is currently seeking...for assigned programs, including interfacing with INPO and Nuclear Regulatory Commission (NRC) as required. + Interacting professionally with… more
- LEGOLAND (Carlsbad, CA)
- …to build your career path is endless! Come join the Team as our Technical Writer , who will support our Rides Maintenance Compliance Team.** **Scope of Job:** + This ... performance management and training. + Document internal and external regulatory requirements into clear, thorough and informative procedures. **Essential… more
- Evolent (Frankfort, KY)
- …both members and providers + Appropriately identifies and refers quality issues to the Senior Director of Medical Management or Medical Director. + ... and communicated clearly **What You Will Be Doing:** The Clinical Letter Writer is responsible for reviewing adverse determination decisions against criteria and… more