- 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
- Houston Methodist (Houston, TX)
- 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 ... 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
- 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
- Terumo Neuro (Aliso Viejo, CA)
- … scientific experience. 3. Demonstrated experience in the development of regulatory / clinical submissions (preferably as a medical writer for pharmaceutical, ... **12933BR** **Title:** Sr. Medical Writer (US Remote & Temp to Hire) **Job...job duties include: + Collaborating with the clinical & regulatory teams to write clinical documents for regulatory… 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
- J&J Family of Companies (Irvine, CA)
- …Johnson & Johnson MedTech, Electrophysiology, is recruiting an **Medical & Technical Writer ** to join our Scientific Operations team. This role can ... Learn more at https://www.jnj.com/medtech As the Medical & Technical Writer within Scientific Operations (SciOps) you will...support to related functions ensuring the delivery of key regulatory and medical documents to gain and retain market… more
- J&J Family of Companies (San Diego, CA)
- …Development **Job Sub** **Function:** Nonclinical Safety **Job Category:** Scientific /Technology **All Job Posting Locations:** San Diego, California, United ... & Johnson Innovative Medicine R&D is recruiting for a Principal Scientist, Nonclinical Submissions Writer . This position is a hybrid role and will be located in San… more
- Abbott (Plano, TX)
- …for a Medical Writer II/ Clinical Evaluation Reporting (CER). The Medical Writer II on our Regulatory Clinical Evaluation team provides technical and ... 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
- Parexel (Frankfort, KY)
- **Company: Parexel is hiring an FSP - Senior Medical Writer with Structured Content Authoring experience to work Remotely.** **Location:** Remote (anywhere in US or ... are dedicated to improving patient lives through innovative clinical research and regulatory solutions. As a leading global clinical research organization (CRO), we… more
- Adecco US, Inc. (Morristown, NJ)
- **Medical Writer (Marketing / Healthcare)** **Adecco Healthcare & Life Sciences** is hiring a **Medical Writer ** on behalf of a leading pharmaceutical partner. ... medical information into clear, audience-appropriate messaging while adhering to regulatory standards. **Pay** 60-69/hr depending on education and experience… more
- Abbott (Maple Grove, MN)
- …for a **Senior Medical Writer , Clinical Evaluation** . The Sr. 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
- Danaher Corporation (Miami, FL)
- …related discipline. . 0-2+ years experience or coursework in technical writing, regulatory affairs, or scientific communication. . Proficiency in Microsoft ... Reagent Labeling Writer Intern Accelerating answers Are you ready to...hands-on experience and exposure in the critical area of regulatory labeling within the medical device and Life Sciences… more
- Parexel (Jefferson City, MO)
- **Job Summary:** The Senior Medical Writer will research, create, and edit all documents associated with clinical research. Responsibilities also include: acting as ... to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator… more
- Danaher Corporation (San Diego, CA)
- …which makes everything possible. The Senior Technical Writer for Leica Biosystems creates accurate, compliant technical ... and support of our products. You will collaborate closely with R&D, Quality, Regulatory , and Service & Support stakeholders to translate complex technical data into… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Development Scientific Director **Location:** Morristown, NJ Cambridge, MA **About the Job** Join the engine of Sanofi's mission - where deep ... that could turn the impossible into possible for millions. The Development Scientific Director (DSD) is a responsible member of the clinical team dedicated… more
- Noblis (Washington, DC)
- Responsibilities **Overview** We are seeking an experienced **Senior Technical Writer /Editor** with a deep understanding of aviation operations, flight procedures, ... NAS operations, and flight procedures** to ensure technical accuracy and regulatory alignment. + Analyze existing and potential content to identify opportunities… more