Selected: âš Scientific Writer.
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đ 2 days ago
Medical Writer developing publications, regulatory documents, and medical communications for WNSâs pharmaceutical and biotechnology clients. Translating complex clinical data into clear, compliant content.
đ Armenia, India â Remote
â° Full Time
đĄ Mid-level
đ Senior
âïž Content Writer
đ» Ghost score 10%
đ 2 days ago
Senior Medical Writer developing medical publications for RTI-HS healthcare research and consulting. Leading publication strategy, client meetings, compliance, and mentoring junior writers.
đČ North Carolina â Remote
đ” $95k - $105k / year
â° Full Time
đ Senior
đ„đ Medical Writer
đ» Ghost score 0%
đ 3 days ago
Senior Medical Writer leading clinical and regulatory document development for ICONâs sponsor-dedicated pharmaceutical research programs in Tokyo or Osaka. Mentoring junior writers and supporting global clinical development.
đ 5 days ago
ICON medical writer developing population PK/PD documents, CSRs, and protocols for sponsor clinical research projects. Ensuring regulatory compliance and inspection-ready deliverables.
đ United Kingdom, France, +8 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ„đ Medical Writer
đ» Ghost score 10%
đ October 23
Senior Medical Writer leading clinical document development and regulatory submissions at ICON Strategic Solutions. Supporting sponsor-dedicated research programs advancing innovative treatments.
đ October 16
Medical Writer preparing and quality-controlling clinical trial documents for Everest, a full-service clinical research organization. Supporting regulatory publications, e-publishing, literature searches, and data monitoring committee administration.
đšđŠ Canada â Remote
đ” $65k - $100k / year
â° Full Time
đą Junior
đĄ Mid-level
đ„đ Medical Writer
đ» Ghost score 1%
đ October 15
Medical Writer authoring clinical and regulatory documents for Quanticate, a global data-focused CRO. Leading projects, supporting clients, and mentoring writers across clinical development programmes.
đźđł India â Remote
âł Contract/Temporary
đĄ Mid-level
đ Senior
đ„đ Medical Writer
đ» Ghost score 12%
đ October 13
Senior Medical Writer leading clinical regulatory document development for TransPerfectâs pharmaceutical and biotech clients in Brazil. Coordinating cross-functional teams, authoring submissions, and managing review cycles.
đ October 13
Senior Medical Writer developing clinical regulatory documents for TransPerfectâs life-sciences clients. Leading cross-functional authoring, reviews, timelines, and regulatory-compliant submissions.
đ October 13
Senior Medical Writer preparing clinical regulatory documents for TransPerfectâs life-sciences clients. Leading protocols, study reports, investigator brochures, and review cycles across France-based remote teams.
đ October 13
Senior Medical Writer preparing clinical regulatory documents for TransPerfectâs life-sciences clients. Leading protocols, study reports, investigator brochures, and cross-functional review cycles.
đ October 13
Senior medical writer leading clinical regulatory document development for TransPerfectâs life-sciences clients. Coordinating authors, reviewers, timelines, and cross-functional stakeholders across Germany.
đ October 13
Senior Medical Writer producing clinical regulatory documents for TransPerfectâs global language-services business. Leading authoring, cross-functional coordination, review resolution, and quality-focused delivery.
đ October 9
Senior Medical Writer developing clinical, nonclinical, and safety documents for argenxâs autoimmune medicine pipeline. Supporting regulatory submissions and inspection-ready medical writing.
đșđž United States â Remote
đ” $128k - $176k / year
â° Full Time
đ Senior
đ„đ Medical Writer
đŠ H1B Visa Sponsor
đ» Ghost score 0%
đ October 7
Senior Medical Writer creating clinical and regulatory documents for Syneos Healthâs life sciences research services. Coordinating reviews, regulatory compliance, and cross-functional study deliverables.
đ October 6
Senior Medical Writer leading clinical trial disclosure submissions at Parexel, a global clinical research organization. Guiding regulatory compliance, client decisions, and junior writer development.
đźđł India â Remote
đ° Venture Round on 1990-01
â° Full Time
đ Senior
đ„đ Medical Writer
đ» Ghost score 17%
đ October 1
Senior Medical Writer preparing clinical regulatory submissions for BeOne, a cancer medicines company. Editing protocols, study reports, and IND, NDA, and MAA documents.
đșđž United States â Remote
đ” $101.7k - $136.7k / year
â° Full Time
đ Senior
đ„đ Medical Writer
đ» Ghost score 0%
đ September 23
Senior Medical Writer preparing regulatory documents and medical communications for Veristatâs life-sciences therapy development programs. Supporting global clinical and regulatory submissions under ICH guidelines.
đ United States, France, +5 more countries â Remote
â°ïž Colorado â Remote
đ° Private equity on 2021-05
â° Full Time
đ Senior
đ„đ Medical Writer
đŠ H1B Visa Sponsor
đ» Ghost score 17%
đ September 17
Medical Writer developing clinical trial documents for Emerald Clinical Trials, a global clinical research company. Drafting protocols, CSRs, regulatory submissions, and scientific manuscripts.
đžđŹ Singapore â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ„đ Medical Writer
đ» Ghost score 15%
đŁïžđšđł Chinese Required
đ September 16
Medical Writer entwickelt wissenschaftlich prĂ€zise Healthcare-Inhalte fĂŒr Ărzte, Fachpersonal und Patienten. BrainersHub treibt als Innovation Hub die digitale Transformation im Gesundheitswesen voran.
đ©đȘ Germany â Remote
đ” âŹ45k - âŹ55k / year
â° Full Time
đĄ Mid-level
đ Senior
đ„đ Medical Writer
đ» Ghost score 12%
đŁïžđ©đȘ German Required
+37 More Scientific Writer Jobs Available!
We analyzed 9 job listings in the last year and found it takes about 36 days for employers to close a job opening.
We reviewed 11 job postings and found the top 10 skills employers are asking for most often are:
You need strong writing and editing skills, proficiency in scientific terminology, and an ability to interpret complex research. Critical thinking, attention to detail, and good time management skills are also essential for remote work.
Typically, you need a degree in a scientific field, such as biology, chemistry, or medicine. Experience in writing for scientific publications and a robust portfolio showcasing your writing skills are highly valuable.
Responsibilities include writing and editing scientific documents, conducting literature reviews, collaborating with researchers to clarify data, ensuring accuracy in scientific content, and adhering to publication guidelines and ethical standards.
Benefits include flexible work hours, the ability to work from any location, reduced commuting time, and improved work-life balance. Remote work also provides opportunities to collaborate with a diverse range of scientists and researchers globally.
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