Senior Medical Writer for AI-Regulatory Docs (Remote)
Ethos
- Remote job
Ethos is working with a leading foundational AI lab to find experienced senior medical writers who can help train their latest language model on professional documents, spreadsheets, and slide deck tasks. We seek candidates with 5+ years in clinical research, biomedical science, or pharma/regulatory affairs to create, evaluate, and refine AI-generated materials across clinical study reports, protocols, investigator brochures, regulatory dossiers, medical affairs slides, and publication plans. #J-18808-Ljbffr Ethos
- ESR Healthcare in New York, NY invites a Medical Writer (Pharmaceutical) to join as a contractor, focused on regulatory writing for AI-assisted clinical documentation. Remote work with NYC placement is offered, aiming for expert judgment across efficacy and safety narratives...Remote jobSeniorRegulatoryFor contractors
$70 - $80 per hour
...firm specializing in IT is looking for a Senior Medical Writer to manage the medical writing function... ...drafting clinical study protocols, regulatory documents, and managing review timelines... ...This full-time position is primarily remote, with a competitive pay range of $70 -...Remote jobSeniorRegulatoryHourly payFull timeContract work$30 - $60 per hour
RemoteJobsOne is seeking a Medical Writer (Pharmaceutical) for a fully remote contract role open to qualified candidates... ...$30 and $60 and emphasizes AI-assisted clinical documentation development... ...model training, with a focus on regulatory quality and accuracy. #J-18808-...Remote jobRegulatoryHourly payContract work- micro1 is a remote, contractor role seeking a Medical Writer (Pharmaceutical) to support AI-assisted clinical documentation projects. You will author and review Clinical Study Reports, safety documents, and regulatory submissions with emphasis on ICH E3 structure and eCTD...Remote jobRegulatoryFor contractors
$100 per hour
...spreadsheets, and slide decks. The role focuses on drafting, reviewing, and refining AI-generated outputs across regulatory filings, risk memos, and policy documents. This flexible remote opportunity offers about 5 to 20 hours per week with a pay rate of $100 per hour,...Remote jobSeniorRegulatoryHourly payImmediate startFlexible hours- ...inVentiv Health Commercial LLC is seeking a Sr Medical Writer Publications to lead the completion of medical writing deliverables remotely. This role involves managing writing activities, ensuring adherence to regulatory standards, and mentoring junior writers. The ideal...Remote workSeniorRegulatory
- ...Leading the development and execution of medical writing strategies for clinical research projects, the full-time remote Senior Medical Writer will manage the preparation and editing... ...skills Strong understanding of regulatory requirements for clinical documents and...Remote workSeniorRegulatoryFull time
- ...supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global... ...Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret...Remote workSeniorRegulatoryWorldwide
- ...Scientific community. We are currently looking for a REMOTE Associate Director Medical Writer to work for a leading San Diego biotech company. Responsibilities... ...with Clinical Development, Biostatistics, and Regulatory teams to translate complex data into clear, high-...Remote workSeniorRegulatoryWork at office
- ...collaborative individual for our medical writing team. The senior medical writer will partner cross-functionally... ...Clinical Operations, Biostatistics, Regulatory, and Program Management in... ...timelines. Location: Fully remote in the US, but must be able to...Remote workSeniorRegulatoryLocal area
- ...Senior Strategic Medical Writer AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues... ...is responsible for leading and writing clinical and regulatory documents for drug and/or device development in support...Remote workSeniorRegulatoryTemporary work
- ...Clinical Regulatory Document Specialist Company Overview Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons' most difficult challenges in...Remote workSeniorRegulatoryInterim roleWorldwide
- ...Senior Medical Writer BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. Guided by our... ...clinical studies and reporting clinical study results for regulatory submissions and publications. Responsibilities: Drafts...Remote workSeniorRegulatoryFull timeFor contractorsShift work
- Syneos Health, Inc. seeks a Senior/Principal Medical Writer with a regulatory focus to lead and manage medical writing deliverables across studies, ensuring... ...junior writers, and maintaining timelines within budget. Remote work is available in the US, UK, and Canada. The role...Remote jobSeniorRegulatory
$145k - $155k
Terumo Group is seeking a Sr. Medical Writer for a remote role in Los Angeles. This position involves collaborating with clinical and regulatory teams to produce a range of medical documents for regulatory submissions, including clinical evaluation reports and study protocols...Remote jobSeniorRegulatory- MMS Holdings Inc is seeking an experienced Medical Writer based in Denver, Colorado. The role involves writing and editing clinical documents... ..., and mentoring team members. A strong background in regulatory writing and at least 3 years of experience in the pharmaceutical...Remote jobSeniorRegulatory
$55 - $75 per hour
A leader in biotechnology is seeking a Senior Medical Writer to draft and manage clinical documentation. This remote contract position offers a competitive hourly rate... ...writing skills, and a deep understanding of regulatory requirements. This role is crucial in supporting...Remote workSeniorRegulatoryHourly payContract work- MMS Holdings Inc is looking for a skilled Medical Writer to join their team in Atlanta, Georgia. The ideal candidate should have a minimum of 3-5 years of experience in regulatory writing within the pharmaceutical industry and possess strong writing capabilities. Responsibilities...Remote jobSeniorRegulatory
- MMS Holdings Inc in Austin, Texas seeks a skilled Medical Writer to evaluate medical literature and write essential clinical documents. Candidates should have 3-5 years of regulatory writing experience within the pharmaceutical industry. The Medical Writer is responsible...Remote jobSeniorRegulatory
- Join MMS, an award-winning data-focused clinical research organization, as a Medical Writer. This full-time, UK-remote role focuses on producing regulatory medical writing deliverables with rigorous scientific standards. You will write and edit protocols, investigator...Remote jobSeniorRegulatoryFull time
- MMS Holdings Inc, based in Michigan, is seeking an experienced Medical Writer to take on critical analysis and writing responsibilities for... .... The ideal candidate will have 3-5 years of experience in regulatory writing and anticipate working closely with clients and project...Remote jobSeniorRegulatory
- Syneos Health, Inc. is seeking a Senior Medical Writer (FSP) with proven experience in clinical document... ...and IBs. The role emphasizes meeting regulatory standards while delivering high-... ...documents on schedule. The position supports remote work with flexibility across EST/CST...Remote jobSeniorRegulatory
- Syneos Health is seeking a Senior Medical Writer Publications - Sponsor Dedicated - Remote Based to lead and manage medical writing deliverables across studies. You will ensure accuracy, maintain regulatory compliance, and mentor junior writers while coordinating with data...Remote jobSeniorRegulatory
- MMS Holdings Inc is seeking a skilled Medical Writer in Chicago. The successful candidate will have a strong background in regulatory writing, including clinical protocols and study reports. They will ensure quality documentation while mentoring fellow team members and...Remote jobSeniorRegulatory
- MMS, a data-focused CRO, is seeking an experienced Medical Writer to critically assess literature, craft clinical development documents, and manage writing projects for regulatory submissions. The role requires leadership of project teams, strong communication with clients...Remote jobSeniorRegulatory
$105k - $125k
...Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Senior Regulatory Medical Writer (FSP ; Remote; US ) At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale...Remote workSeniorRegulatoryTemporary workWork at officeLocal areaFlexible hours- Dropzone AI is seeking a Senior Technical Writer to own how we explain our platform to security teams. You will craft integration guides, admin/docs, API references, and release notes, working with product... ..., accountable team in a fully remote startup. #J-18808-Ljbffr...Remote jobSenior
- MMS Holdings Inc in Baltimore, Maryland is seeking a Medical Writer to critically evaluate and write clinical documents for regulatory submissions. This role demands experience in the pharmaceutical industry and exceptional writing skills to produce high-quality documentation...Remote jobSeniorRegulatory
- ...Defense Solutions, LLC is seeking a Lead Technical Writer to set the direction for the Technical Publications team as it pivots to a docs-as-code model built on Git, Confluence and... ...air-gapped networks. You will champion AI-augmented workflows, mentor writers, and drive...Remote jobSenior
$126.9k - $215.4k
Your Role As the Senior Principal Medical Writer, you will lead the end-to-end development of complex regulatory submission documents—ensuring high communication quality, scientific... ...management. Vendor management and remote leadership. Strong communication, negotiation...Remote workSeniorRegulatory
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