Remote Senior Medical Writer: CSR & Protocols Expert
Regeneron Pharmaceuticals, Inc.
New York, NY
- Remote job
Regeneron Pharmaceuticals, Inc is looking for a Senior Medical Writer to join their Medical Writing team. This role involves authoring clinical documents for Global Development, emphasizing collaboration with clinical teams and biostatisticians. The position also requires mentoring junior staff and contributing to process improvement. The ideal candidate will have a background in medical writing, knowledge of clinical research regulations, and the ability to manage multiple projects from a remote location. #J-18808-Ljbffr Regeneron Pharmaceuticals
Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Remote Senior Medical Writer: CSR & Protocols Expert in New York, NY vacancy
- YO AI Labs is seeking a Medical Writer Expert for a remote contract to develop, review, and evaluate clinical and regulatory documents with scientific... ...regulatory compliance. You will author CSRs, interpret protocols, verify data integrity, and support AI-assisted...Remote jobSeniorContract work
$50 - $80 per hour
YO AI Labs seeks an experienced Medical Writer / Clinical Document Author to develop, review,... ...and high-quality medical writing. This remote contractor role offers an hourly pay rate... ...and reviewing CSRs, interpreting protocols per ICH guidelines, verifying accuracy...Remote jobSeniorHourly payFor contractors- Syneos Health in Remote/NC seeks a Senior Medical Writer with proven clinical document writing experience. You will lead medical writing deliverables, coordinate activities across departments, and ensure compliance with ICH E3 guidelines and client templates. You will mentor...Remote jobSenior
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents... ...CSRs and other regulatory documents, interpret clinical protocols per ICH guidelines, verify data using source data listings,...Remote job
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop... ...medical writing. The role focuses on CSR authoring, protocol interpretation, and rigorous data verification... ...cross-functional collaboration in a remote, contractor capacity. #J-18808-...Remote jobFor 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... ...The role involves authoring CSRs, interpreting protocols per ICH E3, and reviewing safety documentation (...Remote jobContract workFor contractors
- YO AI Labs seeks an experienced Medical Writer / Clinical Document Author to develop, review,... ...accuracy and regulatory compliance. This remote contractor role focuses on high-quality... .... The candidate will interpret protocols, verify data, and support cross-functional...Remote jobFor contractors
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review... ...and regulatory documents, interpret protocols per ICH guidance, verify data, and... ...improvements. This contract role offers remote work with collaboration across global teams...Remote jobContract 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 job
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review... ...involve authoring CSRs, interpreting protocols, and ensuring adherence to ICH E3 and... ...collaboration across cross-functional teams in a remote contractor capacity. #J-18808-Ljbffr...Remote jobFor 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... ...teams. You will author CSRs, interpret protocols, verify data against source documents,...Remote jobFor contractors
- YO AI Labs is seeking an experienced Medical Writer Expert to work remotely on regulatory documentation. You... ...clinical and regulatory manuscripts, CSR authoring, and ensure scientific accuracy... ...compliance. You will interpret protocols, verify data with source documents,...Remote job
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review... ...on authoring CSRs, interpreting protocols per ICH guidelines, and supporting AI‑assisted... ...quality initiatives within a remote contract setting. Strong written communication...Remote jobContract work
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical... ...regulatory compliance for sponsor projects. This remote contractor role focuses on CSR authoring, protocol interpretation, TFL analysis, and eCTD submission...Remote jobFor contractors
- Stryker, a global medical technology leader, seeks a Senior Staff Medical Writer for the Endoscopy Division. The role is remote within the United States and focuses on authoring CERs, PMCF, and regulatory documents to support international registrations and lifecycle management...Remote jobSenior
- Stryker is seeking a Senior Staff Medical Writer for its Endoscopy division. This role can be based remotely anywhere in the United States and focuses on creating and maintaining regulatory documentation, CERs, PMCF, and scientific materials to support global market access...Remote jobSenior
- 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 jobSenior
$50 - $80 per hour
YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop and review... ...across cross-functional teams. Remote contractor position offering $50-$80/hour... ...regulatory medical writing and experience with CSR authoring and clinical study...Remote jobFor 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 jobSeniorContract work
- ...Syneos Health is seeking a Principal / Senior Medical Writer with proven clinical document writing experience. This remote role supports global regulatory deliverables and... ...candidates bring extensive experience with protocols, CSRs, and IBs, and can mentor junior writers...Remote workSenior
Syneos Health Inc
Boston, MA5 days ago - ...pharmaceutical, biotech, and medical device industries with a proven... ...supervision, the Medical Writer will critically evaluate, analyze... ...but not limited to, clinical protocols, investigator’s brochures,... ...various regulatory documents Expert proficiency with client...Remote workSeniorWorldwide
MMS Holdings
Bridgeport, CT2 days ago $145k - $155k
...Sr. Medical Writer Peripheral Vascular Med Device (U.S. Remote) Position Overview This is a Temp-To-Hire Position Primary contact for medical writing... ...experience summaries Investigator brochures Study protocols Medical literature analysis reports Research...Remote workSeniorTemporary workInterim roleTerumo Group
United States4 days ago- MMS is a data-focused CRO seeking an experienced Medical Writer to analyze medical literature, develop regulatory documents, and ensure scientific rigor in study materials. You will draft protocols, study reports, and safety summaries, coordinating with clients and project...Senior
- ...suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing... ...physicians, vendors, and other medical experts. Report on adverse events, complaints... ...documents including but not limited to: protocols, investigational plans, informed consent...Remote workSeniorInterim roleWorldwide
Artivion
United States4 days ago - ...Medical Writing Specialist For the past 25 years... ...including but not limited to: protocols, protocol amendments,... ...experienced medical writers, as necessary.... ...collaborates with subject matter experts in clinical operations... ...ProPharma supports remote working, we also...Remote workSeniorContract workWork at office
ProPharma Group
Chicago, IL1 day ago $126.9k - $215.4k
...Senior Principal Medical WriterWork Your Magic with us! Start your next chapter... ...the Senior Principal Medical Writer, you will lead the end-to-... ...documentation suite (protocols, clinical study reports, Investigator... ...management and remote leadershipStrong communication...Remote workSeniorFlexible hoursEMD Group
North Billerica, MA2 days ago$120k - $159k
...Consulting, a Indegene Company, is hiring Senior/Principal Medical Writers (USA) to support our growing company... ...this time); may work either fully remotely or a hybrid schedule (in office/... ...regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical...Remote workSeniorLive inWork at officeWork visaTrilogy Enterprises
Durham, NC3 days ago$145k - $155k
Terumo Group is seeking a Sr. Medical Writer for a remote role in Los Angeles. This position involves collaborating with clinical and regulatory... ...submissions, including clinical evaluation reports and study protocols. The salary range for this position is $145,000 - $155,000...Remote jobSenior- ...Senior Medical Writer BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. Guided by our... ...conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical...Remote workSeniorFull timeFor contractorsShift work
BioMarin Pharmaceutical
United States1 day ago $110.1k - $183.4k
...Work Flexibility Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely... ...timelines. Author clinical study protocols, study reports, data summaries,... ...Follow‑Up (PMCF) documentation. Expert knowledge of MEDDEV 2.7/1 Rev. 4,...Remote workSeniorFor contractorsWork at officeStryker
Brooklyn, NY3 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Remote Senior Medical Writer: CSR & Protocols Expert. Be the first to apply!
Related searches
- freelance medical writer New York, NY
- medical writer New York, NY
- medical writer remote New York, NY
- senior medical writer New York, NY
- medical editor New York, NY
- freelance medical copywriter New York, NY
- sql expert New York, NY
- subject matter expert New York, NY
- fulfillment expert New York, NY
- guest service support expert New York, NY