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 seeks an experienced Medical Writer/Clinical Document Author to develop, review, and evaluate regulatory documents, ensuring scientific accuracy and regulatory compliance... ...cross-functional teams to drive quality. Remote-friendly environment with emphasis on...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,... ...high-quality medical writing. This is a remote contractor role requiring strong writing...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,... ...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
- 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
- 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
- ...Labs is seeking an experienced Medical Writer / Clinical Document Author to... ..., and evaluate clinical and regulatory documents while ensuring... ...writing. The role focuses on CSR authoring, protocol interpretation... ...collaboration in a remote, contractor capacity. #J-188...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,... ...accuracy with source data, TFLs, and study docs; there is collaboration with cross-...Remote jobRegulatory
- Stryker is hiring a Senior Staff Medical Writer for the Endoscopy Division, remotely anywhere in the United States. The role focuses on developing regulatory and clinical documentation to support global registrations and lifecycle management, partnering with Regulatory...Remote jobRegulatory
- Dart Solutions is seeking a Medical Writer II for a remote role that spans 12 months. The position requires defining and conducting quality control... ...documents while ensuring accuracy and compliance with regulatory submissions. The ideal candidate should possess a Bachelor...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
- 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 jobRegulatoryContract work
- ...with a leading foundational AI lab to find experienced senior medical writers who can help train their latest language model on... ...+ years in clinical research, biomedical science, or pharma/regulatory affairs to create, evaluate, and refine AI-generated materials...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 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
$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 / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents ensuring accuracy and compliance. You... ...improvements. This contract role offers remote work with collaboration across global...Remote jobRegulatoryContract work
- 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
- ...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- ...Job Details: Senior Manager, Medical/Regulatory WriterFull details of the job... ...Manager, Medical/Regulatory Writer || | VN831 || | Full Time ||... ...Gaithersburg, MD, Radnor, PA, Remote, US || | Regulatory Affairs |... ...Authoring clinical study reports (CSR) from individual clinical...Remote workRegulatoryFull timeContract work
$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... ...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- ...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
- ...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
- ...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
- ...Remote Medical Writer Required Skills & Experience: Bachelor's degree in a scientific or engineering field of study; 7+ years of experience... ...in protocol development, writing clinical section for regulatory submission and clinical evaluation report writing; Ability...Remote workRegulatory
$72.9 per hour
...development industry, is seeking a Senior Medical Writer to join their team. As a Sr. Med Writer, you will be part of the Regulatory Affairs department supporting clinical development... ...: Senior Medical Writer Location: 100% Remote (East coast preferred) Pay Range: $72.90/...Remote workRegulatoryWeekly payContract workTemporary workFlexible hours- ...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
- ...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
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