Remote Medical Writer - CSR & Regulatory Docs
YO AI Labs
- Remote job
YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents with a focus on scientific accuracy and regulatory compliance. The role emphasizes high-quality medical writing, CSR authoring, and adherence to ICH guidelines across regulatory submissions. The successful candidate will interpret clinical protocols, verify source data, and collaborate with cross-functional teams, including AI-assisted documentation #J-18808-Ljbffr YO AI Labs
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy,... ...collaboration across cross-functional teams in a remote contractor capacity. #J-18808-Ljbffr YO...Remote jobRegulatoryFor contractors
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop and review regulatory documents with a focus on accuracy and compliance. The role involves interpreting protocols, ensuring ICH E3 alignment, and producing high-quality CSRs and related...Remote jobRegulatory
$70 - $80 per hour
...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 workRegulatoryHourly payFull timeContract work$89k - $148k
...healthcare company is seeking an experienced medical writer to lead projects for Clinical Research... ...interpreting complex research into regulatory documents and mentoring team members.... ...$148,000 annually, plus bonuses, with the potential for remote work. #J-18808-LjbffrRemote workRegulatory- ...Labs is seeking an experienced Medical Writer / Clinical Document Author to develop and review regulatory documents with a focus on... ...compliance. The role emphasizes CSR creation, protocol interpretation... ...contractor position offers remote work and competitive hourly pay...Remote jobRegulatoryHourly payFor contractors
$50 - $80 per hour
...Labs is seeking an experienced Medical Writer / Clinical Document Author to develop and review regulatory documents with scientific... ...across cross-functional teams. Remote contractor position offering $... ...medical writing and experience with CSR authoring and clinical study...Remote jobRegulatoryFor contractors- YO AI Labs is seeking an experienced Medical Writer Expert to work remotely on regulatory documentation. You will develop, review, and evaluate clinical and regulatory manuscripts, CSR authoring, and ensure scientific accuracy and regulatory compliance. You will interpret...Remote jobRegulatory
- Veristat LLC is seeking a full-time Principal Medical Writer to independently plan and prepare regulatory documents and medical communications. This remote role involves supporting all phases of product development while collaborating with cross-functional teams. The ideal...Remote jobRegulatoryFull time
- ...AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop... ...review, and evaluate clinical and regulatory documents, ensuring scientific... ...compliance for sponsor projects. This remote contractor role focuses on CSR authoring, protocol interpretation...Remote jobRegulatoryFor contractors
- YO AI Labs, in a remote contractor engagement, seeks an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents with scientific accuracy and regulatory compliance. The role involves authoring CSRs, interpreting...Remote jobRegulatoryContract workFor contractors
$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... ..., and high-quality medical writing. This remote contractor role offers an hourly pay rate...Remote jobRegulatoryHourly payFor contractors$85k - $98k
...Haymarket Media, Inc. is seeking a Medical Writer to join the PRI team. This... ...team flex day) and two days remote. Job Overview: The Medical... ...participate in client medical/legal/regulatory reviews as needed Maintain an... ...Google Suite such as Slides, Docs in addition to online medical...Remote workRegulatoryWork at officeLocal areaFlexible hours- ...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...Remote workRegulatory
- ...To support clinical research initiatives, the full-time remote Medical Writer will author clinical trial and regulatory documents, engage with cross-functional teams, and ensure document quality and compliance. Key responsibilities Author clinical trial and regulatory...Remote workRegulatoryFull time
- ...Knowesis is seeking a Medical Writer in East Orange, NJ with remote work options to support the VA EXPRT Center. The role involves developing clinical... ...collaboration with multidisciplinary teams and adherence to regulatory standards while advancing research and education #J-1...Remote workRegulatory
- ...development and execution of medical writing strategies for clinical... ...the full-time Senior Medical Writer will manage the preparation... ...with the flexibility to work remotely or onsite. Key responsibilities... ...research, biostatistics, and regulatory affairs to analyze clinical...Remote workRegulatoryFull time
- A leading medical device company is seeking a Medical Writer to develop clinical documents for an innovative project.... ...complex scientific information into regulatory-ready documents. Candidates based... ...encouraged to apply. This is a remote role with an initial contract of...Remote workRegulatoryContract work
- ...Working remotely as a contract Clinical Medical Writer, the candidate will develop high-quality regulatory documents for submission to Sponsors and regulatory agencies, ensuring compliance and scientific rigor. Key responsibilities: Lead the planning, development, and...Remote workRegulatoryContract work
$116k - $128k
...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 proficiency... ..., with various benefits including remote work options and medical insurance. #J-...Remote workRegulatory- ...Medical Writer (Consultant) – Clinical Development / Early Feasibility Study Contract-6-12+Months Seattle, WA- Remote Immediate Need Candidates residing in Europe are also encouraged... ...Ensure alignment with regulatory expectations and submission standards...Remote workRegulatoryContract workImmediate start
- ...Senior Medical Writer Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive... ...our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents...Remote workRegulatoryWork from home
- ...Leads the clear and accurate completion of medical writing deliverables, ensuring... ...scientific meetings. Adheres to established regulatory standards, including but not limited to... ...Mentors and leads less experienced medical writers on complex projects, as necessary....Remote workRegulatoryFlexible hours
- ...Senior Medical Writer/Principal Medical Writer The Senior Medical Writer/Principal Medical... ...Style Guide, Precision SOPs, applicable regulatory guidelines (ie, ICH, FDA, GCP) and eCTD... ...protocols, IBs, ICF templates, DSURs, CSRs, CSR patient narratives with a clear...Remote workRegulatory
- ...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 workRegulatory
- ...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 workRegulatoryWorldwide
- ...Create & maintain plans and reports for regulatory authorities.Review/approve other documentation... ....Must HaveDeep knowledge of EU MDR and Medical Writing from CER, CEP, PMCF Plan &... ...Lafayette, Colorado, or any site in MN, or remote. No requirement to be on site full time...Remote workRegulatoryFull timePart time
- ...Senior Medical Writer This position is listed on behalf of a partner company, who manages... ...Writer based in Brazil. This is a fully remote opportunity for an experienced medical... ...contribute to clinical development and regulatory submission projects. You will...Remote workRegulatoryFull time
- ...Contract Medical Writer (Scientific Communications)At MJH Life Sciences our success is measured... ...(LMR/MRC).Maintain strict attention to regulatory, compliance, and medical accuracy... ...workflow efficiency.Position DetailsLocation: Remote (contract)Contract duration: 6-month...Remote workRegulatoryFull timeContract 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 workRegulatoryInterim roleWorldwide
- ...Senior Medical Writer Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx... ...complex clinical, nonclinical, and safety documents for regulatory submissions. This individual will execute the overall strategy...Remote workRegulatory
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