- Arthrex (Naples, FL)
- …Experience as a clinical research professional and knowledge of clinical regulatory regulations is required. Excellent communication and analytical skills, ... and biomechanical professionals. Arthrex is actively searching for a Clinical Research Technical Writer to join the...purpose of this job is to provide technical and medical writing support for clinical study projects.Essential… more
- MicroVention, Inc. (Tustin, CA)
- …in the development of regulatory / clinical submissions (preferably as a medical writer for pharmaceutical, CRO, or medical device clients). 4. ... **12078BR** **Title:** Sr. Medical Writer **Job Description:** **INNOVATION STARTS...reports, documents and scientific presentations in cooperation with the Clinical , Medical , & Regulatory Affairs… more
- J&J Family of Companies (Horsham, PA)
- Manager, Medical Writer Scientific Communications - 2406180830W **Description** Johnson & Johnson Innovative Medicine is recruiting for a Manager, Medical ... more at https://www.jnj.com/. We are recruiting for a Manager, Medical Writer to join the Scientific Communications...of Biology Editors, as well as ICH and other regulatory guidelines pertaining to study protocols and clinical… more
- Stryker (Cary, IL)
- …will create clear, accurate, and regulatory -compliant documentation related to clinical studies and medical device submissions. + Conduct literature searches ... available at www.stryker.com We are currently seeking a **Staff Medical Writer ** , to join our **...devices, and cosmetics. Interpret and synthesize the information in clinical regulatory documents, in compliance with global… more
- Abbott (St. Paul, MN)
- …and surveillance of changes in Medical Writing per EU and Canada regulatory guidelines. The Principal Medical Writer will provide technical and ... routine fingersticks. **The Opportunity** We are seeking a **Post-Market Safety Evaluation Principal Medical Writer ** to join Abbott's Medical Device on-site… more
- CVS Health (Boston, MA)
- …health care more personal, convenient and affordable. Position Summary The Medical Affairs Clinical Evidence Medical Writer will play a pivotal role to ... with internal best practices, regulatory guidelines, and clinical research and medical writing standards. This...Required Qualifications + 5+ years of experience as a Medical Writer . + Relevant work experience writing… more
- Abbott (Plano, TX)
- …of assigned product manuals. + Collaborates with development engineering, marketing, regulatory affairs, and clinical engineering personnel, among others, to ... instructions for use and other manuals in support of regulatory submissions and product launches. **What You'll Work On**...years of progressively more responsible experience as a technical writer in a medical or high technology… more
- McLaren Health Care (Detroit, MI)
- **Position Summary:** **The Scientific/ Medical Writer ** plays a critical role in the development and execution of Karmanos Cancer Institute (KCI) oncology ... clinical research studies. The primary responsibility of this position...ensure the protocol aligns with the study goals and regulatory requirements. 3. Review and Revision: Regularly review and… more
- System One (Ridgefield, CT)
- …are outsourced to vendors/CROs that are writing clinical trial reports or other clinical regulatory documents and acts as the interface to systems that are ... Job Title: Medical Technical Writer Location: Remote from...Responsibilities + Manages and writes/edits relevant sections of global clinical documents, required for advancing clinical development… more
- University of Miami (Miami, FL)
- … clinical /statistical reports and study protocols.7. Summarizes data from clinical studies for submission to appropriate governmental/ regulatory agencies.8. ... The Sylvester Comprehensive Cancer Center has a great opportunity for a Scientific Writer . The Writer analyzes, simplifies, writes, and designs well - organized,… more
- Houston Methodist (Houston, TX)
- …to the preparation of grant proposals, manuscripts, presentations, protocols, and clinical regulatory documentation. + Assures quality and timely preparation ... At Houston Methodist, the Scientific Writer position is responsible for performing a variety...performing a variety of tasks including preparing laboratory and clinical studies and documents for submission to journals and… more
- Actalent (Conshohocken, PA)
- Seeking 1 Medical Writer HYBRID role- must be commutable to Conshohocken, PA Description: - Drafting and writing clinical study protocols and amendments ○ ... managers, study monitors - Writing for Fast Designation submission - Overseeing regulatory documents ○ Clinical summaries, ISS/ISE, Advisory Committee Briefing… more
- MD Anderson Cancer Center (Houston, TX)
- **Technical Writer ** The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through ... the public. **SUMMARY** Writes, edits and coordinates production of highly technical medical material. Retrieves data from databases and other internal and external… more
- Houston Methodist (Houston, TX)
- …to the preparation of grant proposals, manuscripts, presentations, protocols, and clinical regulatory documentation. + Prepares technical documents that adhere ... At Houston Methodist, the Senior Scientific Writer is responsible for functioning as the mentor...for junior staff with an extensive knowledge of both medical and technical science while working with scientific and… more
- Medtronic (North Haven, CT)
- **Careers that Change Lives** The Senior Medical Writer will partner with the Surgical Scientific Communications Managers & Specialists to support clinical ... be responsible for the creation of scientific documents, including medical writing of clinical study supporting documentation,...on clinical data, from published literature and/or clinical studies, for submission to regulatory agencies… more
- Actalent (Salt Lake City, UT)
- …Technical writing, Medical device, FDA, Sop, Document control, Clinical research, Writing skills, Work instruction, Regulatory documents, Engineering, ... Actalent Services is seeking a Technical Writer to support our Medical Device...Working knowledge of GMP, ISO, and FDA rules and regulatory requirements: Understanding of quality submissions in medical… more
- Belcan (Thousand Oaks, CA)
- …factors, materials science, quality, reliability engineering, domain experts from commercial, clinical , molecular research, medical sciences, regulatory , ... Technical Writer - Life Science Job Number: 347583 Category:...* Background in development, commercialization, and lifecycle management of medical devices * Physical test method development, qualification, and… more
- Teleflex (Olive Branch, MS)
- Technical Writer **Date:** Apr 23, 2024 **Location:** Olive Branch, MS, US **Company:** Teleflex **Expected Travel** : None **Requisition ID** :10103 **About ... Teleflex Incorporated** Teleflex is a global provider of clinically effective medical technologies designed to improve the health and quality of people's lives. We… more
- Abbott (Alameda, CA)
- …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... can grow the career you dream of. + Free medical coverage for employees* via the Health Investment Plan...style, quality, and tone of voice and passes scientific, regulatory , and legal reviews. + You will closely work… more
- Alaka'ina Foundation Family of Companies (Frederick, MD)
- …+ Life, Physical, and Social Science Support - Positions may include: Biostatistician; Clinical Data Manager/ Regulatory Writer ; Quality Assurance Officer; ... Regulatory , Clinical , and Technical Clinical...Scientist; Technical Writer ; Program Manager; Biomedical Science Writer ; Principal Investigator. + Medical Services -… more
