- 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
- 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
- AbbVie (IL)
- …The Principal Medical Writer is responsible for providing clinical regulatory document support and advanced scientific writing expertise to the ... accurate and timely completion/delivery of information and review of clinical regulatory submissions. Serves as the scientific...as medical writing lead on more complex clinical regulatory documents such as those associated… more
- Teva Pharmaceuticals (West Chester, PA)
- …The Senior Medical Writer , in Global Regulatory Medical Writing, writes and edits clinical regulatory documents, including submission ... Senior Medical Writer Date: Apr 23, 2024...Senior Medical Writer Date: Apr 23, 2024 Location: West Chester,...**How you'll spend your day** + Write and edit clinical regulatory documents, including submission summaries and… 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
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …experience in medical writing, publishing and/or editing; AMWA Medical Writer certification a plus + Experience with clinical research; prostate cancer ... clinical study documents including Protocols, Investigator's Brochures, Synopses, Clinical Study Reports, and regulatory documents. + Conduct literature… 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
- 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
- IQVIA (Durham, NC)
- …responding to customer comments with senior support, and staying updated on medical /technical writing and regulatory knowledge, including GCP and advances in ... We are seeking a **Scientific Writer - Vaccines** to join Q2 Solutions, IQVIA's...+ Good understanding of common statistical methods used in clinical trials and/or interpretation of their results, and statistical… 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
- 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
- Boehringer Ingelheim (Ridgefield, CT)
- …continuous risk/benefit assessment. + Authors Investigator Brochures (with support from the Medical Writer and other contributors), Clinical Development ... team ( Clinical Operations, Biostatistics, Translational Medicine, Pharmacovigilance, Regulatory , Medical Affairs, Market Access, Epidemiology, RWE etc)… more
- Pfizer (Pearl River, NY)
- …study statistician, and delivery of clinical study report in collaboration with medical writer and accountable for overall quality and timeliness of analysis ... authorities, key opinion leaders, and principal investigators:** + Supports Clinical Regulatory Authority interactions accountable for providing responses. +… more