Remote Medical Writer: Regulatory Submissions & Reports
Carrot Pharma recruitment
- Remote job
Carrot Life Sciences is partnering with a growing CRO to recruit a Medical Writer. This role blends clinical and regulatory writing with document quality control and publishing, supporting regulatory submissions. You will interpret study results, prepare clinical documents and publications, review for accuracy, manage multiple projects and collaborate with cross-functional teams across pharma and device sectors. #J-18808-Ljbffr Carrot Pharma recruitment
- ...Resources International, Inc. is seeking a Medical Writer in Bethesda, MD to prepare regulatory documents for FDA submissions and scientific reports. The role involves literature reviews,... ...TRI's Bethesda office with 3 days of remote work, offering collaboration with IT...Remote workRegulatoryWork at office
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- ...Job Description Senior Medical Writer - Clinical Development... ...n \n United States / Remote / LA, CA \n \n Our... ...reviewing, and editing regulatory documents required for submission to the U.S. Food and Drug... ...protocols, clinical study reports, and briefing documents....Remote workRegulatoryOdd job
$128k - $160k
...Principal Medical Writer, Regulatory & Scientific Writing Location: Remote or Hybrid in San Diego Employment Type: Full time Reports To: President & Founder About Aroga Aroga... ...control, regulatory operations, and submission management services to...Remote workRegulatoryFull time$78k - $156k
...products in diagnostics, medical devices, nutritionals... ...for a Senior Medical Writer, Clinical Evaluation.... ...Medical Writer on our Regulatory Clinical Evaluation team... ...Clinical Evaluation Reporting documents for the Neuromodulation... ...applications and submissions. Collaborates with...RegulatoryWork experience placementWorldwideShift work- ...Biosciences is seeking a mid-level Regulatory Medical Writer to develop high-quality... ...supporting IND and NDA submissions across drug development programs... ...ready documents. This is a remote-friendly position open to... ...including study reports, protocols and amendments,...Remote workRegulatory
- ...pharmaceutical, biotech, and medical device industries with a... ...approach to complex trial data and regulatory submission challenges. With a global... ...supervision, the Medical Writer will critically evaluate, analyze... ...s brochures, clinical study reports, subject consent forms,...Remote workRegulatoryWorldwide
- ...is seeking a Principal Medical Writer who will lead and deliver... ...for complex clinical and regulatory projects. You will work... ...protocols, clinical study reports, briefing documents, and submission dossiers. Manage end-... ...in multicultural or remote team settings. Proven...Remote workRegulatoryLocal area
- ...domain expertise in regulatory sciences, clinical... ..., medical information, and R... ...narratives, study reports, as well as more complex... ...NDA, BLA, MAA, eCTD submission level documents).... ...experienced medical writers, as necessary.... ...ProPharma supports remote working, we also recognise...Remote workRegulatoryContract workWork at office
- Clin Evaluation Med Writer Job Location: Virtual, MN Duration... ...Clinical Evaluation Medical Writer is responsible for... ...evaluation documents and reports in compliance with regulatory requirements and industry... ...Create responses for audit/submission queries. Required Skills:...Remote jobRegulatoryShift workDay shift
- Principal Medical Writer At Thermo Fisher Scientific, you... ...Europe. This would be a remote role. We are looking... ...edits clinical study reports and study protocols,... ..., document types, regulatory requirements, and therapeutic... ...industry preferred Submissions document experience...Remote workRegulatoryLocal areaFlexible hours
$145k - $155k
Terumo Group is seeking a Sr. Medical Writer for a remote role in Los Angeles. This position... ...with clinical and regulatory teams to produce a range of medical... ...medical documents for regulatory submissions, including clinical evaluation reports and study protocols. The salary...Remote jobRegulatory$65k - $100k
Job Title: Medical Writer Type of company: Full-service Clinical... ...Location: Remote anywhere in Canada, US... ...combines clinical and regulatory writing with document... ...development and regulatory submissions. It's an opportunity... ...clinical study reports, protocols, to name a...Remote workRegulatoryWork at office- ...Holdings Inc is seeking a skilled Medical Writer in Chicago. The successful... ...have a strong background in regulatory writing, including clinical protocols and study reports. They will ensure quality... ...clinical research and regulatory submissions. #J-18808-Ljbffr MMS...Remote jobRegulatory
- ...Emerald Clinical has helped drive medical breakthroughs through deep... ..., including clinical study reports, clinical study protocols,... ...plan outlines, sections of regulatory submission documents, and scientific manuscripts... ...: Enjoy hybrid or remote working arrangements, depending...Remote workRegulatoryLocal areaWorldwide
$132k - $151k
...Description: Job Overview: Regulatory Writers prepare high-quality... ...for regulatory submissions to help streamline... ...clients. The Principal Medical Writer (PMW) is a major... ...culture - 70% remote workforce, 66% women-... ...documents to create summary reports Expertise to provide...Remote workRegulatoryLocal areaWorldwideFlexible hours- Senior Medical Writer At ICON Strategic Solutions, you will... ...clinical and regulatory documents in collaboration... ...Protocols or Clinical Study Reports . This includes Phase... ...that documents are submission-ready and finally... ...processes. #LI- remote #LI-NR1 What ICON can...Remote workRegulatoryWorldwideFlexible hours
- ...exciting opportunity for a Medical Writer ! Key Accountabilities :... ...finalize clinical documents for submission to regulatory authorities, including but... ...and final clinical study reports, common technical document... ...Related Sciences or equivalent. #LI-KW1 #LI-REMOTE PAREXELRemote workRegulatoryInterim roleFlexible hours
$145k - $155k
Sr. Medical Writer Peripheral Vascular Med Device (U.S. Remote) Position Overview This is a Temp-To-Hire... ...with the clinical & regulatory teams to write clinical... ...documents for regulatory submissions, including but not... ...Clinical evaluation reports Interim and final clinical...Remote jobRegulatoryTemporary workInterim role$90k - $100k
...Summary: The Senior Medical Writer serves as an integral... ...or San Francisco-or remotely within the US, depending... ..., and support Veeva submissions of all medical... ...client medical/legal/regulatory reviews by highlighting... ...position has no direct reports and does not perform...Remote workRegulatoryWork experience placementCasual workWork at officeLocal areaNight shiftWeekend work2 days per week- ...professionals specializing in medical writing, submission publishing, and... .... Synterex offers remote or on‑site services,... ...The senior medical writer will partner cross‑... ..., Biostatistics, Regulatory, and Program Management... ...publications, study reports, investigator...Remote workRegulatoryLocal area
$80.6k - $175.7k
Senior Medical Writer (FSP) - Clinical document writing experience... ...: Today Location: Remote, MO, United States... ...; clinical study reports; patient narratives;... ...development plans; IND submissions; integrated summary reports... ...to established regulatory standards, including,...Remote workRegulatoryContract workFlexible hours- Sr Principal Medical Writer job at ICON Strategic Solutions. Remote. Sr. Principal Medical Writer ICON... ...-quality clinical and regulatory documents, ensuring clarity... ...clinical study reports, protocols, investigator... ...brochures, and regulatory submissions. Ensuring all documents...Remote jobRegulatoryFlexible hours
- ...innovation. Job Title: Medical Writer Location: United States (Remote) Function: Drug Safety DESCRIPTION... ...limited to aggregate reports (e.g., Development... ...Reports/ ACO/ DSUR) for submission to local and other Health... ...Exposure in handling regulatory agency/ Pharmacovigilance...Remote workRegulatoryHourly payContract workFor contractorsWork at officeLocal areaFlexible hours
- ...the most innovative medical minds together with the... .... Our Medical Writer will have the overall... ...material. This is a remote position based in the... ...associated with submissions to regulatory authorities, including... ..., and Clinical Study Reports Serve as the Medical...Remote workRegulatoryFull timeWork experience placementWork at officeRelocation package
$55 - $75 per hour
...with significant unmet medical need. We enlist the best... ...is a Contract role- Remote can live anywhere in the... ...hour The Senior Medical Writer applies advanced documentation... ...clinical studies and reporting clinical study results for regulatory submissions and publications....Remote workRegulatoryFull timeContract workFor contractorsWorldwideShift work$85k - $98k
...Media, Inc. is seeking a Medical Writer to join the PRI team.... ...day) and two days remote. Job Overview: The... ...will also assist with submissions of work to a client’s... ...client medical/legal/regulatory reviews as needed... ...Complete and submit expense reports on time Skills &...Remote workRegulatoryWork at officeLocal areaFlexible hours- micro1 is a remote, contractor role seeking a Medical Writer (Pharmaceutical) to support AI-assisted clinical documentation projects... ...will author and review Clinical Study Reports, safety documents, and regulatory submissions with emphasis on ICH E3 structure and eCTD...Remote jobRegulatoryFor contractors
- ...community. We are currently looking for a REMOTE Associate Director Medical Writer to work for a leading San Diego... ...Development, Biostatistics, and Regulatory teams to translate complex data... ..., comment resolution, and on-time submission readiness • Ensure all...Remote workRegulatoryWork at office
- ...Make an Impact as a Medical Writer II at Worldwide To be considered... ...developing high-quality clinical and regulatory documents that contribute to... ...You'll Work This is a REMOTE role open to candidates... ..., assents, clinical trial reports, narratives, and Investigator...Remote workRegulatoryWork at officeWorldwideNight shift
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