Remote Contract: Regulatory Medical Writer — CSR Expert
YO AI Labs
- Remote job
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 protocols per ICH E3, and reviewing safety documentation (DSURs/PSURs/PBRERs). You will provide structured feedback and support AI-assisted quality initiatives. #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... ...quality initiatives within a remote contract setting. Strong written communication...Contract workRemote jobRegulatory
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to... ..., review, and evaluate clinical and regulatory documents ensuring accuracy and compliance... ...documentation quality improvements. This contract role offers remote work with collaboration across...Contract workRemote jobRegulatory
- 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-...Contract workRemote jobRegulatory
$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
- 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 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
- ...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 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...Contract workRemote 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
- ...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
$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- ...Details: Senior Manager, Medical/Regulatory WriterFull details of... ..., Medical/Regulatory Writer || | VN831 || | Full... ...Gaithersburg, MD, Radnor, PA, Remote, US || | Regulatory... ...of all external (contract) writers contributing... ...clinical study reports (CSR) from individual clinical...Contract workRemote workRegulatoryFull time
- ...seeks an experienced Biostatistician for contract-based work supporting clinical research projects... ...data, validating outputs, and ensuring regulatory compliance using SAS and R. Responsibilities include SAP review, TFL production, CSR evaluation, and cross-functional...Contract workRemote jobRegulatory
- ...Job Title Provides high-quality regulatory medical and scientific writing in support of Phase... .... Reviews documents prepared by junior writers and peers. May provide training and mentorship... ...timelines, budgets, forecasts, and contract modifications, as well as identifying...Contract workRemote workRegulatory
- A global medical device consulting firm is looking for a EUMDR Medical Writer for a remote, full-time engagement. Candidates should have a minimum of 5 years of medical or... ..., literature reviews, and compliance with regulatory guidelines. Strong written and oral communication...Remote jobRegulatoryFull time
- A leading medical device company is seeking a Medical Writer to develop clinical documents for an innovative... ...scientific information into regulatory-ready documents. Candidates... ...encouraged to apply. This is a remote role with an initial contract of 6-12 months. #J-18808-...Contract workRemote jobRegulatory
- ...Sr Medical Writer Publications - Sponsor Dedicated - Remote Based Syneos Health is a leading fully integrated biopharmaceutical... .... Adheres to established regulatory standards, including, but not... ...to create an employment contract. Occasionally, required skills/experiences...Contract workRemote workRegulatoryFlexible hours
- 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 jobRegulatory
- ...Description: Principal Medical Writer The Principal Medical Writer... ...and prepares a range of regulatory documents and medical... ...Flexible, inclusive culture - 70% remote workforce, 66% women-led teams... ...writing experience in a contract research organization or pharmaceutical...Contract workRemote workRegulatoryWork at officeWorldwideFlexible hours
$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 -...Contract workRemote jobRegulatoryHourly payFull time$50 - $80 per hour
...week for our client. The position is fully remote. Responsibilities Leading the sale and... ...the full process from marketing through contract execution. Developing and implementing a... ...ensuring compliance with company and regulatory requirements. Coordinating with transformer...Contract workRemote workRegulatoryHourly payFor contractors10 hours per week- Crossing Hurdles is seeking a Medical Writer / Clinical Document Author on a contract basis to support AI tool development. This remote role requires strong regulatory medical writing experience and the ability to author or lead full Clinical Study Reports. You will review...Contract workRemote jobRegulatory
- ...Medical Writing Specialist For the past... ...domain expertise in regulatory sciences, clinical... ...experienced medical writers, as necessary.... ...with subject matter experts in clinical operations... ...diagnostics for a contract research... ...ProPharma supports remote working, we also recognize...Contract workRemote workRegulatoryWork at office
$90k - $130k
...Medical Writer Biodesix is a leading diagnostic solutions company,... ...authors, and subject matter experts to develop publication strategies... ...policies, and applicable regulatory requirements. Operates independently... ..., pharmaceuticals, contract research organizations,...Contract workRemote workRegulatoryTemporary workImmediate start$80.6k - $175.7k
...Description Principal Medical Writer - Publications Syneos Health... ...• Adheres to established regulatory standards, including, but not... ...appropriately. • Serves as expert peer reviewer for internal... ...construed to create an employment contract. Occasionally, required...Contract workRemote workRegulatoryFlexible hours$172k - $232.8k
...The Principal Medical Writ er (equivalent to Associate Director) represents medical... ...Procedures (SOPs), and oversees the work of contract writers on the clinical program as well as... ...the sponsor/CRO setting. Experience with regulatory submissions (NDA/BLA/MAA) strongly...Contract workRemote workRegulatoryFull timeTemporary workFor contractorsLocal areaFlexible hours$90k - $140k
...Senior Medical Writer Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad... ...Canada on-site location, or remotely from a home-based office anywhere... ...documents supporting regulatory submissions for clinical trial...Contract workRemote workRegulatoryTemporary workWork from homeWorldwide- ...seeking a Bio/Sterile Drug Product Process Expert to oversee sterile manufacturing at CMOs,... ...and timely investigations. This 12-month contract role emphasizes technical leadership, cross-functional collaboration, and regulatory readiness. The ideal candidate has a strong...Contract workRemote jobRegulatory
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