Remote Medical Writer: CSR & Regulatory Documents
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 ensuring scientific accuracy and regulatory compliance. This remote contractor role focuses on CSRs, regulatory submissions, and quality-controlled medical writing. Responsibilities include interpreting protocols, performing source data verification, reviewing DSURs/PSURs, and contributing to AI-assisted documentation initiatives while collaborating #J-18808-Ljbffr YO AI Labs
- YO AI Labs seeks an experienced Medical Writer / Clinical Document Author for a remote contractor role to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy and regulatory compliance. You will author and review CSRs, interpret...Remote jobDocumentRegulatoryFor contractors
- ...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 jobDocumentRegulatoryHourly payFor contractors
- ...is seeking an experienced Medical Writer / Clinical Document Author to develop, review,... ...and evaluate clinical and regulatory documents while ensuring scientific... .... The role emphasizes CSR authoring, protocol... ...functional teams within a remote contractor setting. Oncology...Remote jobDocumentRegulatoryFor contractors
- 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 jobDocumentRegulatory
- 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 CSRs, interpret...Remote jobDocumentRegulatory
$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 jobDocumentRegulatoryFor 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 jobDocumentRegulatoryFor 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 jobDocumentRegulatory
- 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 jobDocumentRegulatory
- 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 jobDocumentRegulatoryContract work
- 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 and regulatory compliance. The role involves authoring CSRs, interpreting protocols per...Remote jobDocumentRegulatory
- 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 jobDocumentRegulatory
- ...is seeking an experienced Medical Writer / Clinical Document Author to develop, review,... ...and evaluate clinical and regulatory documents while ensuring scientific... .... The role focuses on CSR authoring, protocol... ...functional collaboration in a remote, contractor capacity. #J-...Remote jobDocumentRegulatoryFor contractors
- ...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 jobDocumentRegulatoryFor 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 jobDocumentRegulatoryContract 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 jobDocumentRegulatoryHourly payFor contractors- ...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 workDocumentRegulatory
- ...Knowesis is seeking a Medical Writer in East Orange, NJ with remote work options to support the VA EXPRT Center... ...developing clinical and research documents, educational outreach, and quality... ...multidisciplinary teams and adherence to regulatory standards while advancing...Remote workDocumentRegulatory
- A leading medical device company is seeking a Medical Writer to develop clinical documents for an innovative project. This role focuses on... ...scientific information into regulatory-ready documents. Candidates... ...encouraged to apply. This is a remote role with an initial...Remote workDocumentRegulatoryContract work
- ...development and execution of medical writing strategies for... ...-time Senior Medical Writer will manage the... ...review of clinical study documents, collaborate with... ...the flexibility to work remotely or onsite. Key responsibilities... ..., biostatistics, and regulatory affairs to analyze...Remote workDocumentRegulatoryFull time
- ...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 workDocumentRegulatoryFull time
$70 - $80 per hour
...specializing in IT is looking for a Senior Medical Writer to manage the medical writing... ...involves drafting clinical study protocols, regulatory documents, and managing review timelines within... ...This full-time position is primarily remote, with a competitive pay range of $70...Remote workDocumentRegulatoryHourly payFull timeContract 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 workDocumentRegulatoryContract work
$116k - $128k
...Strategies, LLC is looking for a Senior Medical Writer specializing in clinical documentation. This role involves leading... ...'s degree and over 3 years of regulatory writing experience. A strong proficiency... ...with various benefits including remote work options and medical...Remote workDocumentRegulatory- ...Medical Writer (Consultant) – Clinical Development / Early Feasibility Study... ...Contract-6-12+Months Seattle, WA- Remote Immediate Need Candidates... ...SME input and manage document versioning Ensure alignment with regulatory expectations and submission standards...Remote workDocumentRegulatoryContract workImmediate start
$89k - $148k
...healthcare company is seeking an experienced medical writer to lead projects for Clinical... ...involves interpreting complex research into regulatory documents and mentoring team members. Qualified... ...8,000 annually, plus bonuses, with the potential for remote work. #J-18808-LjbffrRemote workDocumentRegulatory- ...About the job Medical Writer 37554294 Remote Medical Writer, 7 Months Contract Sigma Systems is currently looking for a Remote Medical... ...the development of high-quality clinical and regulatory documents that support global clinical development programs. This...Remote workDocumentRegulatoryContract work
- ...Senior Medical Writer Are you looking to join a company where your contributions truly matter... ...approach to complex trial data and regulatory submission challenges. With a global footprint... ...Write and edit clinical development documents, including but not limited to, clinical...Remote workDocumentRegulatoryWork from home
- ...Senior Medical Writer/Principal Medical Writer The Senior Medical Writer... ...and on-time clinical study documents. Specific responsibilities... ...Precision SOPs, applicable regulatory guidelines (ie, ICH, FDA, GCP... ...ICF templates, DSURs, CSRs, CSR patient narratives with a...Remote workDocumentRegulatory
- ...Managing clinical program documents for assigned clients, the full-time Principal Medical Writer will independently author high-... ...completion of projects while working remotely. Key responsibilities... ...edits clinical, safety, and regulatory documents across various therapeutic...Remote workDocumentRegulatoryFull time
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