Remote Clinical Medical Writer for 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 while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. This is a remote contractor role requiring strong writing and cross-functional collaboration. Responsibilities include authoring Clinical Study Reports, interpreting protocols per ICH guidelines, verifying data with source data, and supporting AI-assisted #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 with a focus on scientific accuracy... ...emphasizes high-quality medical writing, CSR authoring, and adherence to ICH guidelines...Remote jobRegulatory
- ...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... ...documentation quality initiatives within a remote contract setting. Strong written...Remote workRegulatoryContract workTemporary work
- 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
- 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 Expert to develop, review, and evaluate clinical and regulatory documents remotely as a contractor. The role emphasizes scientific accuracy, regulatory compliance, and collaboration with cross-functional teams. You will...Remote jobRegulatoryFor contractors
- 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, regulatory compliance, and high-quality medical writing. You will author and review CSRs...Remote jobRegulatory
- Sumitomo Pharma America, Inc. is seeking a QC Medical Writer to perform QC audits of clinical regulatory documents and support the Medical Writing team. This role... ...and documents meet company standards. Primarily remote with periodic on-site meetings; travel domestically...Remote jobRegulatory
- ...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
$70 - $80 per hour
...specializing in IT is looking for a Senior Medical Writer to manage the medical writing function. The role involves drafting clinical study protocols, regulatory documents, and managing review... ...full-time position is primarily remote, with a competitive pay range of $70...Remote jobRegulatoryHourly payFull timeContract work- YO AI Labs is seeking a Medical Writer Expert for a remote contract to develop, review, and evaluate clinical and regulatory documents with scientific precision and regulatory compliance. You will author CSRs, interpret protocols, verify data integrity, and support AI-...Remote jobRegulatoryContract work
- 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...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- ...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
$85k - $98k
...Media, Inc. is seeking a Medical Writer to join the PRI team.... ...day) and two days remote. Job Overview: The Medical... ...Assess and ensure clinical accuracy of all content... ...client medical/legal/regulatory reviews as needed Maintain... ...Suite such as Slides, Docs in addition to online...Remote workRegulatoryWork at officeLocal areaFlexible hours- ...health research institute is seeking an experienced Source Writer with QA/QC/Regulatory expertise. You will ensure high standards of scientific... ...documents, performing QA reviews, and ensuring compliance with clinical research regulations. The ideal candidate will have a...Remote jobRegulatory
- ...Cabaletta Bio is seeking a Manager, Medical Writer and Quality Control Specialist for remote work to support regulatory affairs and clinical development. This role partners with clinical and regulatory teams to produce high-quality documentation for regulators, editors...Remote workRegulatory
- ...Working remotely in a full-time capacity, the Medical Writer will analyze and interpret safety results from clinical trials, compile and write clinical study reports, and ensure compliance with regulatory standards. Key responsibilities Analyze and interpret various...Remote workRegulatoryFull time
- ...and experienced in pharmaceutical advertising, the Medical Editor will provide project-based support remotely, focusing on editing and proofreading promotional... ...reference source materials to support medical/legal/regulatory (MLR) review Collaborate with copywriters,...Remote workRegulatory
- ...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
- ...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 and research documents, educational outreach... ...teams and adherence to regulatory standards while advancing research...Remote workRegulatory
- ...development and execution of medical writing strategies for clinical research projects, the full-time Senior Medical Writer will manage the... ...the flexibility to work remotely or onsite. Key responsibilities... ...research, biostatistics, and regulatory affairs to analyze...Remote workRegulatoryFull time
- A leading medical device company is seeking a Medical Writer to develop clinical documents for an innovative project. This role focuses... ...scientific information into regulatory-ready documents. Candidates... ...encouraged to apply. This is a remote role with an initial contract...Remote workRegulatoryContract work
- ...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... ...MMS is an award-winning, data-focused clinical research organization (CRO). We pride... ...scientific approach to complex trial data and regulatory submission challenges. With a global...Remote workRegulatoryWork from home
$45 - $50 per hour
...Medical Editor We're looking for a detail-driven Medical Editor to support project-based... ...30 hours per week when work comes in Remote, EST Responsibilities: Edit and... ...materials to support medical/legal/regulatory (MLR) review Ensure claims are properly...Remote workRegulatoryHourly payFull timeContract workFreelance$50.45k - $56.05k
Initial Disclosure Specialist I (Docs & Funding) Compensation: $50,445 - $56,050 Base... ...while ensuring compliance with applicable regulatory requirements. This role works closely with... ...benefits package, including medical, dental, vision, paid time off, paid holidays...Remote jobRegulatory- ...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
- ...About the job Medical Writer 37554294 Remote Medical Writer, 7 Months Contract Sigma Systems is currently looking for a Remote... ..., and coordinating the development of high-quality clinical and regulatory documents that support global clinical development...Remote workRegulatoryContract work
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