- ThermoFisher Scientific (Greenville, NC)
- …Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Principal Medical Writer ** At Thermo Fisher Scientific , you'll discover meaningful ... growing, and we are looking for a Principal Medical Writer . This role is based in the United States....research. Your expertise will enable us to deliver flawless Regulatory Medical Writing documents, such as protocols, CSR, Investigator… more
- Nanobiosym, Inc. (Cambridge, MA)
- Cambridge, MA, USA | Contract Job Title: Scientific Writer (Onsite Consultant)Location: Cambridge, MA About the Role: We are seeking an experienced Scientific ... Writer with a strong background in scientific editing and publication to support our research and communications team. The ideal candidate will have a PhD or… more
- University of Miami (Miami, FL)
- …of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Hybrid Scientific Writer 2 to work at the UHealth medical campus in Miami, Fl. ... CORE JOB SUMMARYThe Hybrid (1X a week or as necessary) Scientific Writer 2 collects and analyzes complex scientific data and concepts within a variety of… more
- Houston Methodist (Houston, TX)
- The Houston Methodist Peak Brain & Pituitary Tumor Center seeks a scientific writer . The scientific writer will primarily be responsible for proofreading ... ESSENTIAL FUNCTIONS** + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills… more
- ThermoFisher Scientific (Greenville, NC)
- …Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **FSP Senior** ** Regulatory ** **Medical Writer (** **Remote;** **US** **)** At ... based in the US! As a remote-based Senior Medical Writer within the FSP team, you will provide high-quality...the FSP team, you will provide high-quality medical and scientific writing from planning and coordination through delivery of… more
- University of Miami (Miami, FL)
- …experimental) for comprehensive analysis, assisting in the preparation of scientific manuscripts, presentations, and regulatory submissions. This list ... application templates for grant proposals. Formats substantive copy and scientific editing, proofreading, and finalizing documents as required and requested.… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- **Job Description Summary** The Medical Writer develops scientific and medical communication materials within BD Diagnostic Solutions (DS), collaborating with ... Writer , Medical Communications (MedComms) **Position Summary** : The Medical Writer develops scientific and medical communication materials within BD… more
- United Therapeutics (Research Triangle Park, NC)
- …You Are You are creative and detail-oriented with deep expertise in regulatory submissions and writing, including clinical study reports, clinical study protocols, ... and investigator's brochures. You also bring strong experience in external-facing scientific communications - such as manuscripts, posters, and abstracts - to… more
- Terumo Medical Corporation (Somerset, NJ)
- … presentations preferred . + Demonstrated experience in the development of regulatory /clinical submissions, preferably as a medical writer for pharmaceutical, ... Sr. Medical Writer Date: Nov 18, 2025 Req ID: 5154...Somerset, NJ, US, 08873 Company: Terumo Medical Corporation Department: Scientific Data & Communication **Job Summary** Combining knowledge of… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director-Principal Medical Writer **Location:** USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for ... skills could be critical in helping our teams accelerate progress. The Principal Medical Writer is a key member of the Medical Writing team, the Clinical Trial Team… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …writing skills, and a proven ability to translate complex clinical and scientific data into clear, accurate, and regulatory -compliant documents tailored to ... to the Vice President of Clinical Development, the Medical Writer will be responsible for leading and executing all...+ Develop and authora broad range of clinical and regulatory documents, including but not limited to: clinical study… more
- System One (New Brunswick, NJ)
- …Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and ... Job Title: Pharma Technical Writer Location: New Brunswick, NJ Hours/Schedule: Mon-Friday (normal...to project timelines and aligned with CTD requirements and regulatory strategy. + Provide input and scientific … more
- J&J Family of Companies (Spring House, PA)
- …Development **Job Sub** **Function:** Nonclinical Safety **Job Category:** Scientific /Technology **All Job Posting Locations:** San Diego, California, United ... Innovative Medicine R&D is recruiting for a Senior Principal Scientist, Nonclinical Submissions Writer . This position is a hybrid role and can be located in Spring… more
- Sanofi Group (Morristown, NJ)
- **Medical Writer ** **Location:** US, Morristown, NJ / M Station **Job type:** Full time **About you:** Sanofi is seeking a highly organized, detail-oriented Medical ... Writer to join our team. In this role, you will develop regulatory -compliant clinical documents supporting our product lifecycle while embracing innovative… more
- Stryker (Cheyenne, WY)
- **Staff Medical Writer (Remote)** We are currently seeking a **Staff Medical Writer ** to join our **Sports Medicine Business Unit** , part of the **Stryker ... this role, you will collaborate closely with cross-functional teams, including Regulatory , Clinical, Quality, and Marketing to ensure the successful preparation of… more
- Bristol Myers Squibb (San Diego, CA)
- …to join our growing clinical development team. This hybrid role combines the scientific writing of key clinical and regulatory documents with oversight of ... + Author, edit, QC, and publish high-quality clinical and regulatory documents in accordance with ICH, GCP, and company...managing medical writing projects or acting in a lead writer role. + Experience with oncology products required and… more
- System One (Cleveland, OH)
- …related scientific discipline + Minimum of 6+ years of pharmaceutical regulatory medical writing and 3+ years of scientific /academic writing experience, and ... Job Title: Director / Senior Director Medical Writer Location: CST or EST candidates willing to...will include the successful preparation of high quality, submission-ready regulatory documents, reports and protocols through implementation of the… more
- Abbott (St. Paul, MN)
- …for a Clinical Evaluation Reporting / Medical Writer (CER). The Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic ... products. Experience in clinical study management and design, medical, or scientific writing, and/or quality engineering/risk management and strong written and… more
- Flywheel Partners (New York, NY)
- …Collaborate with a multi-functional account team to develop innovative medical and scientific educational materials tailored to our clients' needs. The audiences for ... affairs. + Writing/Content Development + Research, learn, and simplify complex scientific /medical information, ensuring it is clearly communicated to the target… more
- University of Utah (Salt Lake City, UT)
- …**Job Title** Research Scientist **Working Title** Research Scientist, Protocol Writer **Career Progression Track** F **Track Level** **FLSA Code** Professional ... **Job Summary** Develops research projects and is responsible for scientific design, conduct and interpretation, presenting results and publishing manuscripts.… more