Remote Medical Writer - Clinical Study Reports
Crossing Hurdles
- Remote job
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 evaluation tasks, ensure clinical template compliance, and provide structured rationales to improve AI model behavior, collaborating with project leads across multiple therapeutic areas including oncology and haematology. #J-18808-Ljbffr Crossing Hurdles
$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 teams to produce a range of medical... ..., including clinical evaluation reports and study protocols. The salary range for this position...Remote job- Celerion is seeking a Medical Writer to work remotely. The role analyzes and interprets safety results from clinical trials, compiling, writing and editing clinical study reports and other industry documents. It requires accurate classification of events and medications...Remote job
- ...Job Description Job Title: Medical Writer IV Location: Santa Clara, CA (remote) Contract Duration: 1 year... ...currently have an opportunity for a Clinical Evaluation Reporting / Medical Writer (CER) for... .... Experience in clinical study management and design, medical...Remote workContract workWork experience placement
$110.1k - $183.4k
...hiring a Senior Staff Medical Writer to join our... ...Division, to be based remotely anywhere within the United... ...develop scientific and clinical documentation that supports... ...Clinical Evaluation Reports (CERs), Post-Market Clinical... ...from clinical studies, published literature,...Remote workFull time- ...Senior Medical Writer Are you looking to join a company where your contributions... ...award-winning, data-focused clinical research organization (CRO).... ...materials for adequate study design, statistical... ...'s brochures, clinical study reports, subject consent forms, integrated...Remote workWork from home
- SGS in Richardson, TX is seeking a technical writer to draft protocols and reports for clinical studies on cosmetics or other claims, ensuring alignment with ICH and GCP guidelines. You will coordinate internal and external protocol reviews, maintain templates and SOPs...
$69k - $115.5k
...Clinical Research/Academic Writing Support In this role you will be providing medical writing services and consultation to Clinical Research Scientists, Academic partners... ..., investigator brochures, clinical study reports, informed consent forms, etc.) and presentations...Remote workShift work- ...Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to... ...Leading the preparation and review of clinical study reports, protocols, and other regulatory documents to...Remote work
- ...Principal Medical Writer ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving... ...the preparation and review of clinical study reports, protocols, and other regulatory documents...Remote workFlexible hours
- ...Senior Medical Writer When our values align, there's no limit to what we can achieve... ...improve the world's health. From clinical trials to regulatory, consulting,... ...regulatory documents, including Study Protocols, Clinical Study Reports (CSRs), Investigator Brochures (IBs...Remote work
$211k - $264k
...seeking a motivated individual with a clinical regulatory writing background to... ...team leadership responsibilities, reporting to the Executive Director, Medical Writing. This position is... ...processes and work instructions, medical writer onboarding materials, and style...Remote workFull timeContract workLocal areaWorldwide- ...Medical Writer II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients... ...of clinical data (e.g., from clinical study reports, safety summaries, biostatistical tables, published...Remote work
- ...Medical Writing Specialist For the past 25 years... ...regulatory sciences, clinical research solutions, quality... ...protocol amendments, study reports, patient narratives,... ...less experienced medical writers, as necessary.... ...Whilst ProPharma supports remote working, we also recognize...Remote workContract workWork at office
- ...Senior Medical Writer- ICON- Remote USA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments... ...of clinical data (e.g., from clinical study reports, safety summaries, biostatistical tables,...Remote work
$105k - $125k
...Description Senior Regulatory Medical Writer (FSP ; Remote; US ) At Thermo Fisher... ...delivery of life-changing therapies. With clinical trials conducted in 100+ countries and... ...clinical documents such as clinical study reports and study protocols and summarizes data...Remote workTemporary workWork at officeLocal areaFlexible hours- ...execution of tactics. Conceptualizes and develops medical communications for message-driven, concise reviewer-friendly clinical documents in order to support regulatory... ...ordinates writing and reviews of clinical trial reports, narratives, clinical trial protocols, local...Remote workLocal area
- Senior Medical Writer I 12 Months FTC I Fully Remote I Based in EU A leading global clinical research organization is seeking a Senior or Principal Medical Writer... ..., review, and editing of clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs)...Remote workFixed term contract
- Precision Medicine Group seeks a Senior Medical Writer/Principal Medical Writer to lead development of clinical study documents with high quality and on-time delivery. The role emphasizes planning, writing, editing, formatting, and QC across protocols, IBs, ICFs, DSURs,...Remote job
- INC Research is seeking a Senior Medical Writer to support clinical study and regulatory project teams. This position is home based anywhere in the US. The ideal candidate will mentor junior writers while managing complex medical writing tasks across various therapeutic...Remote jobWork from home
- ...Associate Director/Principal Medical Writer The Principal... ...Writing team, the Clinical Trial Team (CTT) and Project... ...States (this is remote but confirmation of current... ...individual clinical studies. Main... ...coordination, in English, of reports and/or related regulatory...Remote workContract workFor contractorsWork experience placementLocal areaWorldwide
- Medical Writer (Consultant) - Clinical Development / Early Feasibility Study Contract-6-12+Months Seattle, WA- Remote Immediate Need Candidates residing in Europe are also encouraged to apply. Overview We are seeking an experienced Medical Writer to support the initial...Remote workContract workImmediate start
$96.2k - $151.4k
...The Clinical and Regulatory Strategic Communications (CRSC) department within Global... ...facing materials. The Health Literacy Medical Writer, in collaboration with a project lead,... ...clinical regulatory (e.g., clinical study reports, participant narratives, investigator’...Full timeFor contractorsWork at officeLocal area$96.2k - $151.4k
Job Description The Clinical and Regulatory Strategic Communications (CRSC) department... ...facing materials. The Health Literacy Medical Writer, in collaboration with a project lead,... ...clinical regulatory (e.g., clinical study reports, participant narratives, investigator’...Work at officeLocal areaRelocationVisa sponsorshipFlexible hoursShift work$78k - $156k
Position Details Senior Medical Writer - Clinical Evaluation Reporting (CER) job at Abbott. Maple Grove, MN. Job ID: 31158618 Posted: Posted 5 Days Ago Start Date: 2026-08-11 Location: United States - Minnesota - Maple Grove, United States of America Time Type: Full time...Full timeWork experience placementWorldwideShift work- ...Stryker is hiring a Senior Staff Medical Writer for the Endoscopy Division, remotely anywhere in the United States.... ...on developing regulatory and clinical documentation to support... ...You will author CERs, PMCF, study protocols and reports, conduct literature reviews, and...Remote work
$119.3k - $159.3k
...Medical Writing Position BeOne continues to grow at a rapid pace with... ...high-quality, fit-for-purpose clinical and regulatory documents to... ...but are not limited to, clinical study protocols, investigator brochures, clinical study reports, regulatory briefing documents,...Remote workHourly payFull timeFor contractorsLocal area- ...pharmaceutical, biotech, and medical device industries with... ..., the Medical Writer will critically evaluate... ...materials for adequate study design, statistical significance... ...bias Write and edit clinical development documents,... ..., clinical study reports, subject consent forms,...Remote workWorldwide
- ...Senior Medical Writer/Principal Medical Writer Remote, United Kingdom Position Summary: The Senior Medical... ...of high-quality and on-time clinical study documents. Specific responsibilities... ...recruitment scam, we encourage you to report the incident to your local law...Remote workLocal area
$119.3k - $159.3k
...high-quality, fit-for-purpose clinical and regulatory documents to facilitate... ...are not limited to, clinical study protocols, investigator brochures, clinical study reports, regulatory briefing documents,... ...(eg, meetings of DIA and medical writing communities) with guidance...Remote workHourly payFull timeFor contractorsLocal area- ...Medical Writer Position We're looking for a brilliant individual to join our team as a Medical Writer who demonstrates an excellent scientific... ...as part of a project call where required Attends and reports on conferences and external meetings, as required...Remote workWork at office
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