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
$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 workSeniorRegulatoryHourly payFull timeContract work- Synterex, Inc. is seeking a senior medical writer to lead planning and preparation of high-quality regulatory documents within our medical writing team. You will partner across Clinical Development, Regulatory, and Program Management to deliver protocols, study reports,...Remote jobSeniorRegulatory
- ...MMS Holdings Inc is seeking an experienced Medical Writer located in Bridgeport, Connecticut, to support the pharmaceutical and biotech... ...clinical development documents and requires a strong background in regulatory writing alongside exceptional writing and organizational...Remote workSeniorRegulatory
- ...Syneos Health is seeking a Principal / Senior Medical Writer with proven clinical document writing experience. This remote role supports global regulatory deliverables and cross-functional collaboration across study teams and clients. Ideal candidates bring extensive experience...Remote workSeniorRegulatory
- ...Stryker is hiring a Senior Staff Medical Writer to join the Endoscopy Division. This remote role supports the US market for regulatory and scientific documentation throughout the product lifecycle. Based in the United States, you will author CERs, PMCF, and other clinical...Remote workSeniorRegulatory
- ...development and execution of medical writing strategies for... ...research projects, the full-time Senior Medical Writer will manage the preparation... ...the flexibility to work remotely or onsite. Key responsibilities... ..., biostatistics, and regulatory affairs to analyze clinical...Remote workSeniorRegulatoryFull time
$50 - $80 per hour
...YO AI Labs seeks an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance... ...-quality medical writing. This remote contractor role offers an hourly...Remote workSeniorRegulatoryHourly payFor contractors$116k - $128k
...Information Strategies, LLC is looking for a Senior Medical Writer specializing in clinical documentation... ...Bachelor's degree and over 3 years of regulatory writing experience. A strong... ...bonuses, with various benefits including remote work options and medical insurance. #J...Remote workSeniorRegulatory- ...Senior Medical Writer/Principal Medical Writer The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development... ...with Precision MW Style Guide, Precision SOPs, applicable regulatory guidelines (ie, ICH, FDA, GCP) and eCTD requirements. The...Remote workSeniorRegulatory
$145k - $155k
...Sr. Medical Writer Peripheral Vascular Med Device (U.S. Remote) Position Overview This is a Temp-To-Hire Position Primary contact for medical writing... ...duties include: Collaborating with the clinical & regulatory teams to write clinical documents for regulatory...Remote workSeniorRegulatoryTemporary workInterim role- Stryker is seeking a Senior Staff Medical Writer for its Endoscopy division, based remotely in the United States. You will lead regulatory documentation, CER/PMCF preparation, and evidence synthesis to support registrations and lifecycle management. You will collaborate...Remote jobSeniorRegulatory
- ...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
- 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
$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- ...Senior Medical Writer When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide...Remote workSeniorRegulatory
- ...Senior Medical WriterSynterex, Inc. is a global consortium of highly experienced... ...support. Synterex offers remote or on-site services, with a... ...team. The senior medical writer will partner cross-... ...Operations, Biostatistics, Regulatory, and Program Management in leading...Remote workSeniorRegulatoryLocal area
- ...maintain plans and reports for regulatory authorities.Review/approve... ...HaveDeep knowledge of EU MDR and Medical Writing from CER, CEP, PMCF... ..., or any site in MN, or remote. No requirement to be on site... ...Influence: Communicates with senior internal and external customers...Remote workSeniorRegulatoryFull timePart time
$95k - $125k
...Senior Medical Writer, Medical Communications Remote, United States Are you passionate about transforming complex science into meaningful, impactful... ...strong domain knowledge across therapeutic areas, regulatory standards, and key statistical concepts You are...Remote workSeniorRegulatory- MMS Holdings Inc in Boston is seeking a Medical Writer to evaluate medical literature and prepare clinical documents, including clinical... ...and study reports. This role requires at least 3-5 years of regulatory writing experience in the pharmaceutical industry. The ideal...Remote jobSeniorRegulatory
- ...Senior Strategic Medical WriterAbbVie's mission is to discover and deliver innovative medicines and solutions... ...Aesthetics portfolio.The Senior Strategic Medical Writer is responsible for leading and writing clinical and regulatory documents for drug and/or device...Remote workSeniorRegulatoryTemporary work
- YO AI Labs seeks an experienced Medical Writer Expert for remote contract work. You will develop, review, and evaluate clinical and regulatory documents with a focus on accuracy, regulatory compliance, and quality. This role requires deep expertise in CSRs, ICH guidelines...Remote jobSeniorRegulatoryContract work
- ...biopharmaceutical solutions company is seeking a Sr Medical Writer to lead medical writing deliverables and ensure compliance with regulatory standards. Responsibilities include... ...writing and ICH guidelines. The role is remote-based and offers competitive benefits such...Remote jobSeniorRegulatoryFlexible hours
- 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
- Stryker is hiring a Senior Staff Medical Writer for the Endoscopy Division. This role is based remotely within the United States, collaborating with Regulatory Affairs, Clinical Affairs, Quality, R&D, and Marketing to translate complex clinical data into regulatory and...Remote jobSeniorRegulatory
- Stryker in the United States is seeking a Senior Staff Medical Writer for the Endoscopy Division, to be based remotely across the U.S. You will develop scientific and regulatory documents to support global registrations and lifecycle management. You will work with Regulatory...Remote jobSeniorRegulatory
- 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
- ...Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions... ...regulations and standards as applicable Writing clinical regulatory documents including annual reports, study summaries, and other...Remote workSeniorRegulatoryInterim roleWorldwide
- 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
- A leading data-focused CRO is seeking a Remote Senior Medical Writer to contribute to clinical development documents and mentor team members. Candidates should have strong writing skills, at least three years of experience in the pharmaceutical industry, and an educational...Remote jobSeniorRegulatoryFull time
$120k - $159k
...Consulting, a Indegene Company, is hiring Senior/Principal Medical Writers (USA) to support our growing company in producing regulatory documentation for the international... ...visa at this time); may work either fully remotely or a hybrid schedule (in office/remote) from...Remote workSeniorRegulatoryLive inWork at officeWork visa
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