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Medical Writer (5605766)
BioPoint - Cambridge, MA
Briefing document for protocol assistance (non-similarity report):. At least 2 years experience clinical experience doing standard regulatory medical writing...
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Scientific Report Writer
A Chicago-based Toxicology Testing & Research Laboratory - Chicago, IL
Prior experience in writing reports for pre-clinical toxicity studies is a plus. A private, Chicago-based contract toxicology testing and research laboratory,...
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Regulatory Medical Writer- Medical Device
HealthCare Recruiters International - Boston, MA
Ability to understand and interpret statistical results of clinical studies; Screens articles against inclusion/exclusion criteria, extracts data from included...
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Senior Medical Writer

Medtronic - 728 reviews - Mansfield, MA
Write and edit Clinical Evaluation Reports, Clinical Summaries, including special summaries from raw data for submission to regulatory agencies, adverse event...

Part-time Senior Medical Writer

Medtronic - 728 reviews - Mansfield, MA
And edit Clinical Evaluation Reports, Clinical Summaries, including. Study Reports, Protocols, abstracts and manuscripts....

Medical Writer (Onsite OR Home Based)

Planet Pharma - Bethesda, MD
Experience in Clinical Study Reports and Integrated Summaries of Efficacy and Safety:. Ideally 5+ years experience in Clinical Study Reports and Integrated...
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Medical and Scientific Writer

USA16 - US - Q2Solutions - Ithaca, NY
Competence in completing good first draft technical reports or clinical reports within a reasonable timeframe with limited guidance....

Senior Medical Writer

Eli Lilly - 579 reviews - Indianapolis, IN
Experience in clinical development, clinical trial process or regulatory activities. Experience writing regulatory, clinical trial documents and or publications...

Medical Writer

Cytokinetics - South San Francisco, CA 94080
Expertise regarding Clinical Study Report (CSR) and appendices. Protocols/amendments, investigator brochures, consent forms, annual reports, DSURs, final study...

Senior Medical Writer - Remote

MMS Holdings Inc. - Thousand Oaks, CA 91358  +4 locations
Write and edit clinical development documents, including but not limited to, clinical protocols, investigator's brochures, clinical study reports, subject...

Clinical Study Lead

Galderma Laboratories, LP - Fort Worth, TX 76101 (Downtown area)
Takes responsibility for the Clinical Study Report (CSR) development, and collaborates with the scientific writer....

Senior Medical Writer

Stemcentrx - South San Francisco, CA
Write, edit and facilitate the review of clinical study reports, study protocols, investigator’s brochures, clinical data summaries, and other medical...
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Medical Writer III (Clinical Science)

Hologic - 57 reviews - United States
Clinical plans, clinical study protocols and reports, integrated summaries, package insert text relating to clinical studies, responses to FDA and regulatory...
Senior Tecnical Scientific Writer
Private Multinational BioPharmaceutical Co. - Hauppauge, NY
Specifically, write clinical study reports, clinical study protocols and amendments*. You can interpret clinical and non-clinical data in the preparation of...
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Senior Medical Writer, Regulatory Writing
INC Research - 76 reviews - United States
Clinical study reports; Clinical study protocols and clinical protocol. Medical writer on clinical study or regulatory project teams....
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