Remote Medical Writer Jobs
136 Medical Writer jobs available for remote work from home. Apply for positions such as Associate Medical Writer, Medical Writer - Regulatory Writing Associate, RWE Senior Medical Writer and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Associate Medical Writer supports the scientific services team by developing accurate technical content such as slide decks, manuscripts, and digital materials. They also manage project timelines, participate in status calls, and maintain high-quality standards through proactive research and internal collaboration.
The Regulatory Writing Associate serves as a lead writer for regulatory documents such as protocols and clinical study reports while managing project timelines. They also facilitate document review meetings with cross-functional teams and ensure the accuracy and consistency of all deliverables.
The Senior Medical Writer is responsible for preparing clinical study documents such as protocols, informed consent forms, and study reports for late-phase and RWE projects. They also develop scientific communications like manuscripts and posters while ensuring quality control and providing statistical interpretation support.
Lead the planning, authoring, and lifecycle maintenance of clinical study reports and clinical evaluation reports to support global regulatory submissions. Collaborate with cross-functional teams to ensure scientific accuracy, traceability, and alignment with regulatory requirements.
The Principal Medical Writer will lead the development of high-quality clinical and regulatory documents, including CSRs, IBs, and ICFs. They will also manage complex projects, mentor colleagues, and build strong relationships with clients and cross-functional teams.
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The Regulatory Writing Associate serves as a lead writer for regulatory documents such as protocols and clinical study reports while managing project timelines. They also facilitate document review meetings with cross-functional teams and ensure the accuracy and consistency of all deliverables.
The Senior Regulatory Writing Specialist will serve as the lead writer for key regulatory documents such as protocols, CSRs, and briefing books. They will also manage project timelines, lead cross-functional review meetings, and ensure the accuracy and consistency of all regulatory deliverables.
The Principal Medical Writer develops high-quality complex clinical and regulatory documents while ensuring compliance with global regulatory standards. They also provide senior-level review, mentorship to junior staff, and lead process improvement initiatives within the FSP team.
The associate medical writer is responsible for researching and developing technical medical materials while ensuring accuracy and adherence to editorial standards. They will also liaise with clients and medical experts while attending scientific meetings to support content development.
Develop high-quality scientific content for medical communications projects, adapting it to client strategy, therapeutic areas, and target audiences while meeting deadlines and budgets. Manage day-to-day client communication, present work and proposal sections, keep project teams informed of relevant developments, and contribute to conferences and external meetings as needed.
Develop and oversee high-quality medical communications deliverables, including clinical publications, slide decks, scientific platforms, symposia, advisory boards, and training materials. Provide final review and sign-off for assigned accounts, ensuring scientific accuracy, appropriate interpretation of data, and strong editorial quality.
The Medical Writer is responsible for planning, coordinating, and delivering high-quality medical and scientific documents such as clinical study reports and protocols. They collaborate with internal and external clients to ensure operational excellence and compliance with regulatory requirements.
The Senior Medical Writer is responsible for producing high-quality medical and scientific documentation while managing project timelines, budgets, and external partnerships. They provide advisory support to scientific teams and ensure operational excellence through effective planning and technical coordination.
The Senior Medical Writer is responsible for authoring and maintaining critical clinical documentation such as Clinical Evaluation Plans and Reports in compliance with EU MDR and MEDDEV regulations. They also collaborate with cross-functional teams to analyze clinical data and ensure high standards of quality and regulatory compliance across all deliverables.
The Senior Medical Writer is responsible for drafting and reviewing essential study documents such as protocols, informed consent forms, and study reports. They also develop scientific communications and provide quality control for deliverables while collaborating with cross-functional teams.
Write and edit clinical and safety documents for pharmaceutical and medical device development, including protocols, informed consent documents, clinical study reports, CTDs, DSURs, and PBRERs, as well as manuscripts and abstracts. Manage document projects in direct response to client needs and collaborate with medical, statistical, clinical operations, and regulatory teams.
The Contract Medical Writer is responsible for researching, creating, and editing clinical trial documentation including protocols, investigator brochures, and regulatory submissions. They collaborate with cross-functional teams to ensure document compliance with regulatory standards and internal SOPs throughout the clinical trial lifecycle.
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Develop high-quality scientific and medical materials such as manuscripts, posters, and slides while ensuring strategic alignment and scientific accuracy. Provide mentorship to scientific writers and collaborate with internal and external stakeholders to meet client needs.
The Senior Medical Writer leads the preparation of regulatory submission documents, including protocols, amendments, and clinical study reports, while ensuring scientific accuracy and adherence to regulatory standards. They also coordinate document reviews, mentor junior staff, and collaborate with cross-functional teams to meet project timelines and budgets.
The role involves leading the preparation of regulatory medical writing deliverables, including protocols, amendments, and clinical study reports. The writer will collaborate with clinical scientists and cross-functional teams to ensure scientific accuracy and adherence to regulatory standards.
The Associate Medical Writer supports the Clinical Services team by writing, revising, and annotating promotional medical content. They are responsible for conducting literature reviews, organizing references, and ensuring the accuracy of scientific claims in accordance with brand guidelines.
The Associate Medical Writer supports the Clinical Services team by writing, revising, and annotating promotional medical content. They are responsible for conducting literature reviews, organizing references, and ensuring the accuracy of scientific claims in accordance with brand guidelines.
Develop regulatory submission documents in accordance with global guidelines and manage medical writing projects across cross-functional teams. Provide input on deliverables, mentor junior staff, and participate in process improvement initiatives.
Review and quality-check medical content by referencing existing text and images against relevant scientific literature, and research studies and information on assigned topics. Write medical and scientific content for websites, emails, and submission materials, collaborating with writers, consultants, creative teams, and clients in briefings and project meetings.
The Medical Writer is responsible for developing scientifically rigorous and strategically aligned medical content for pharmaceutical and life science clients. They manage the day-to-day content development process, ensuring accuracy and adherence to brand style guides and project timelines.
The role involves leading the preparation of clinical study protocols and amendments while partnering closely with clinical scientists. The writer will manage medical writing deliverables, ensure regulatory compliance, and coordinate quality reviews across departments.
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The Medical Writer will critically evaluate medical literature and write/edit complex clinical development documents such as protocols, study reports, and regulatory submissions. They will also manage project timelines, interact directly with clients, and mentor other team members.
The Medical Writer develops scientifically accurate and strategically aligned content for medical affairs and promotional medical education deliverables. They collaborate with creative and digital teams to translate complex clinical data into clear messaging while ensuring compliance with regulatory and MLR standards.
The Associate Director leads the development of clinical regulatory documents and provides strategic direction to cross-functional teams. They are responsible for ensuring high-quality, data-driven submissions to global regulatory authorities while mentoring less experienced staff.
Develop regulatory documents for global submissions in accordance with ICH guidelines and manage medical writing projects across cross-functional teams. Participate in process improvement initiatives and mentor junior medical writing staff to ensure high-quality deliverables.
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The average salary for remote Medical Writers is $94,360 per year. This is based on data from 11 job openings. We use the yearly salaries in US dollars from these job postings to calculate salary expectations. Below is a breakdown of salary data by years of experience:
| Experience | Salaries counted | Average salary |
|---|---|---|
| Entry-level0–2 years | 4 | $71,250 |
| Junior2–5 years | 4 | $89,053 |
| Senior5–10 years | 3 | $132,250 |
We reviewed 54 job postings for remote Medical Writers and found these are the skills employers ask for most often:
| Skill | Share of job posts |
|---|---|
| Medical writing | 91% |
| Project management | 65% |
| Scientific writing | 46% |
| Clinical study reports | 37% |
| Mentoring | 30% |
| Quality control | 24% |
| Cross-functional collaboration | 24% |
| Microsoft Word | 22% |
| Regulatory compliance | 22% |
| Clinical research | 22% |
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