Remote Medical Writer Jobs
Remote medical writer jobs are open across the U.S. at remote-first pharmaceutical companies, distributed clinical research organizations, and digital health firms that rely on medical writers to produce regulatory documents, clinical content, and patient-facing materials. Employers hiring remotely right now include Veristat, サイネオス・ヘルス, and Precision Medicine. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 44+ Remote Medical Writer jobs
About Perceptive
Our mission is to shape the future of clinical research. With decades of experience and the brightest minds in the industry, we help the global biopharmaceutical industry bring new, advanced medical treatments to market, faster.
We seek to change the world, and with the support of our teams across the globe, we flourish together. At Perceptive, we are one team. We learn, grow and win together.
Are you ready to help change the world?
Apart from job satisfaction, we can offer you:
- Medical, Dental and Vision benefits for you and your family, including Flexible Spending Accounts (FSA) and Health Savings Accounts (HSAs)
- Paid time off policy including holidays and sick time
- Internal growth and development programs & trainings
WEALTH:
401(k) program, life & accident insurance and disability insurance
About the role
A Senior Medical Writer will create, research, edit and coordinate the production of clinical documents related to independent review, including independent review charters, clinical data forms, manual case report forms, applicable reviewer training materials, project deviations and supplementary imaging reports, either independently or using available central content and templates. The medical writer will serve as a contact with clients.
Key Accountabilities:
Information Content authoring
- Gather, review, analyze, and evaluate relevant resources to prepare, develop, and finalize applicable clinical documents for submission to regulatory authorities.
- Prepare, develop, and finalize applicable clinical documents not intended for submission to regulatory authorities.
- Revise document drafts based on the review comments from team members to ensure inclusion of all relevant input.
- Follow required standard operating procedures (SOPs), templates, guidelines, regulations, client instructions, and other processes, as applicable.
- Perform literature searches/reviews as necessary to obtain background information and training for development of documents.
- Draft and/or ghost-write clinical documents for more experienced medical writers
- Act as support to others in the team to ensure that all documentation is accurate and encompasses all relevant information based on Stakeholder needs.
- Initiate and participate in departmental or interdepartmental process improvement and training initiatives, including development of departmental SOPs, central content, and general guidelines for clinical documentation and workflow procedures. Initiate and participate in marketing initiatives, such as white paper, abstract, poster, and manuscript development
Document Project Management
- Serve as primary client contact for medical writing projects, negotiating deliverable timelines, and resolving project-related issues.
- Serve as the medical writing representative on assigned project teams communicate content requirements, lead/facilitate authoring team meetings to agree on expectations
- Coordinate and conduct interdepartmental team reviews of draft and final documents,
- Evaluate progress on tasks, identify issues and facilitate resolutions, and advance document development to approval, according to Perceptive and/or client guidelines/SOPs.
- Distribute final documents to project team and client in a timely manner and to agreed timescales
- Identify potential project challenges and raise with all relevant stakeholders, including changes in timelines or out of scope requests, and suggest possible resolution options.
- Attend project team meetings as required.
- Ensure appropriate filing of applicable project documentation May provide project management of contractual and financial aspects.
Relationship management
- Implements stakeholder engagement/communications plan.
- Deals with problems and issues, managing resolutions, corrective actions, lessons learned and the collection and dissemination of relevant information.
- Collects and uses feedback from customers and stakeholders to help measure effectiveness of stakeholder management. Helps develop and enhance customer and stakeholder relationships.
Quality management
- Uses appropriate methods and a systematic approach in the development, maintenance, control and distribution documents.
- Prepares documents for publishing readiness, ensuring document consistency and integrity
- Ensures documentation adheres to FDA/EMA or other appropriate regulatory guidelines, and / or relevant SOPs.
- Provides medical editing review of draft and final documents prepared by other medical writers before internal or external distribution. This includes both copyediting and content review.
- Follows required standard operating procedures (SOPs), templates, guidelines, regulations, client instructions, and other processes, as applicable. Makes changes to and controls the updates and distribution of quality standards.
Relationship management
- Implements stakeholder engagement/communications plan.
- Deals with problems and issues, managing resolutions, corrective actions, lessons learned and the collection and dissemination of relevant information.
- Collects and uses feedback from customers and stakeholders to help measure effectiveness of stakeholder management. Helps develop and enhance customer and stakeholder relationships.
Other
Carryout any other reasonable duties as requested.Skills:
- Excellent interpersonal, verbal, presentational and written communication skills
- Ability to consistently produce documents of high quality
- A flexible attitude with respect to work assignments and new learning
- Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
- Must have the ability to work methodically in a fast-paced, time-sensitive environment
- Demonstratable ability to apply critical thinking to problems and tasks
- Shows initiative and self-confidence, is adaptable and is able to cope with changing and evolving priorities
- Ability to identify and implement process improvements
- Proactively participates in skills improvement training and encourages their teams to participate
- Ability to negotiate on behalf of medical writing to ensure resources, timelines, and expectations are aligned
- Maintains an up-to-date awareness of trends, tools, technology, techniques, processes and documentation requirements that affect technology within the Life sciences domain
- A self-starter and able to work under own initiative Proven ability of using Microsoft Office products (including Word, Excel & PowerPoint)
Knowledge and Experience:
- Experience using tools to communicate progress to Stakeholders
- Experience of regulated environments
- Understanding of Agile methodologies
- Experience of working in and knowledge of the life sciences sector
- Solid knowledge of industry guidelines and regulations, i.e., ICH-GCP.
- Experience of regulatory documents in a contract research organization, pharmaceutical or biotechnology firm, or some experience in the conduct of clinical research/medical communications.
- Solid Professional experience in the same or very similar role
- Experience using data analysis tools (e.g. Tableau, Power BI) desirable Proven ability of using Microsoft Office products (including Word, Excel & PowerPoint)
Education:
- Bachelor's Degree in a technical discipline (Science, pharmacy, nursing, or other health-related discipline preferred etc.) or a related study, or equivalent project-related experience
- English: Fluent (written and verbal) Non-English language (Written and verbal) desirable
-
This role is remote US based. Candidates located in the following states: AZ, CT, DE, FL, GA, IL, MA, MO, NH, NJ, NC, PA, UT, VA are preferred. The annual base salary range for this role is $84,368-$120,526. This range represents the anticipated initial annual salary and will vary depending on several factors including the candidate’s experience and skills as well as market rate adjustment.
Come as you are.
We're proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, colour, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
About Perceptive
Our mission is to shape the future of clinical research. With decades of experience and the brightest minds in the industry, we help the global biopharmaceutical industry bring new, advanced medical treatments to market, faster.
We seek to change the world, and with the support of our teams across the globe, we flourish together. At Perceptive, we are one team. We learn, grow and win together.
Are you ready to help change the world?
Apart from job satisfaction, we can offer you:
- Medical, Dental and Vision benefits for you and your family, including Flexible Spending Accounts (FSA) and Health Savings Accounts (HSAs)
- Paid time off policy including holidays and sick time
- Internal growth and development programs & trainings
WEALTH:
401(k) program, life & accident insurance and disability insurance
About the role
A Senior Medical Writer will create, research, edit and coordinate the production of clinical documents related to independent review, including independent review charters, clinical data forms, manual case report forms, applicable reviewer training materials, project deviations and supplementary imaging reports, either independently or using available central content and templates. The medical writer will serve as a contact with clients.
Key Accountabilities:
Information Content authoring
- Gather, review, analyze, and evaluate relevant resources to prepare, develop, and finalize applicable clinical documents for submission to regulatory authorities.
- Prepare, develop, and finalize applicable clinical documents not intended for submission to regulatory authorities.
- Revise document drafts based on the review comments from team members to ensure inclusion of all relevant input.
- Follow required standard operating procedures (SOPs), templates, guidelines, regulations, client instructions, and other processes, as applicable.
- Perform literature searches/reviews as necessary to obtain background information and training for development of documents.
- Draft and/or ghost-write clinical documents for more experienced medical writers
- Act as support to others in the team to ensure that all documentation is accurate and encompasses all relevant information based on Stakeholder needs.
- Initiate and participate in departmental or interdepartmental process improvement and training initiatives, including development of departmental SOPs, central content, and general guidelines for clinical documentation and workflow procedures. Initiate and participate in marketing initiatives, such as white paper, abstract, poster, and manuscript development
Document Project Management
- Serve as primary client contact for medical writing projects, negotiating deliverable timelines, and resolving project-related issues.
- Serve as the medical writing representative on assigned project teams communicate content requirements, lead/facilitate authoring team meetings to agree on expectations
- Coordinate and conduct interdepartmental team reviews of draft and final documents,
- Evaluate progress on tasks, identify issues and facilitate resolutions, and advance document development to approval, according to Perceptive and/or client guidelines/SOPs.
- Distribute final documents to project team and client in a timely manner and to agreed timescales
- Identify potential project challenges and raise with all relevant stakeholders, including changes in timelines or out of scope requests, and suggest possible resolution options.
- Attend project team meetings as required.
- Ensure appropriate filing of applicable project documentation May provide project management of contractual and financial aspects.
Relationship management
- Implements stakeholder engagement/communications plan.
- Deals with problems and issues, managing resolutions, corrective actions, lessons learned and the collection and dissemination of relevant information.
- Collects and uses feedback from customers and stakeholders to help measure effectiveness of stakeholder management. Helps develop and enhance customer and stakeholder relationships.
Quality management
- Uses appropriate methods and a systematic approach in the development, maintenance, control and distribution documents.
- Prepares documents for publishing readiness, ensuring document consistency and integrity
- Ensures documentation adheres to FDA/EMA or other appropriate regulatory guidelines, and / or relevant SOPs.
- Provides medical editing review of draft and final documents prepared by other medical writers before internal or external distribution. This includes both copyediting and content review.
- Follows required standard operating procedures (SOPs), templates, guidelines, regulations, client instructions, and other processes, as applicable. Makes changes to and controls the updates and distribution of quality standards.
Relationship management
- Implements stakeholder engagement/communications plan.
- Deals with problems and issues, managing resolutions, corrective actions, lessons learned and the collection and dissemination of relevant information.
- Collects and uses feedback from customers and stakeholders to help measure effectiveness of stakeholder management. Helps develop and enhance customer and stakeholder relationships.
Other
Carryout any other reasonable duties as requested.Skills:
- Excellent interpersonal, verbal, presentational and written communication skills
- Ability to consistently produce documents of high quality
- A flexible attitude with respect to work assignments and new learning
- Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
- Must have the ability to work methodically in a fast-paced, time-sensitive environment
- Demonstratable ability to apply critical thinking to problems and tasks
- Shows initiative and self-confidence, is adaptable and is able to cope with changing and evolving priorities
- Ability to identify and implement process improvements
- Proactively participates in skills improvement training and encourages their teams to participate
- Ability to negotiate on behalf of medical writing to ensure resources, timelines, and expectations are aligned
- Maintains an up-to-date awareness of trends, tools, technology, techniques, processes and documentation requirements that affect technology within the Life sciences domain
- A self-starter and able to work under own initiative Proven ability of using Microsoft Office products (including Word, Excel & PowerPoint)
Knowledge and Experience:
- Experience using tools to communicate progress to Stakeholders
- Experience of regulated environments
- Understanding of Agile methodologies
- Experience of working in and knowledge of the life sciences sector
- Solid knowledge of industry guidelines and regulations, i.e., ICH-GCP.
- Experience of regulatory documents in a contract research organization, pharmaceutical or biotechnology firm, or some experience in the conduct of clinical research/medical communications.
- Solid Professional experience in the same or very similar role
- Experience using data analysis tools (e.g. Tableau, Power BI) desirable Proven ability of using Microsoft Office products (including Word, Excel & PowerPoint)
Education:
- Bachelor's Degree in a technical discipline (Science, pharmacy, nursing, or other health-related discipline preferred etc.) or a related study, or equivalent project-related experience
- English: Fluent (written and verbal) Non-English language (Written and verbal) desirable
-
This role is remote US based. Candidates located in the following states: AZ, CT, DE, FL, GA, IL, MA, MO, NH, NJ, NC, PA, UT, VA are preferred. The annual base salary range for this role is $84,368-$120,526. This range represents the anticipated initial annual salary and will vary depending on several factors including the candidate’s experience and skills as well as market rate adjustment.
Come as you are.
We're proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, colour, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
See All 44 Remote Medical Writer Jobs
Find roles that match your experience and apply in just a few clicks.
Find Remote Medical Writer JobsRemote Medical Writer Job Market
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Science & Research
- Healthcare & Medical Services
- Consulting & Professional Services
What Employers Look For
The qualifications that appear most often in remote medical writer jobs.
- Bachelor's or advanced degree in life sciences, pharmacy, or a related scientific field
- Demonstrated experience writing clinical study reports, regulatory submissions, or medical communications
- Proficiency with Microsoft Word styles, templates, and tracked-changes workflows
- Familiarity with ICH guidelines, FDA or EMA submission requirements, and Good Documentation Practice
- Strong ability to interpret and translate clinical data for scientific and non-scientific audiences
- American Medical Writers Association certification (AMWA) or equivalent credential preferred
Tips for Your Remote Medical Writer Job Search
Build a portfolio of document types
Remote employers want to see that you can produce clinical study reports, regulatory submissions, or patient education materials without hand-holding. Include at least two or three document types in your portfolio to show range and self-sufficiency before you apply.
Apply early to remote roles that fit
Migrate Mate lists remote medical writer openings from across the U.S. in one place, so you can find roles matched to your background and apply directly without sorting through unrelated listings.
Signal your async communication skills clearly
Remote medical writing teams depend on written handoffs, version-controlled documents, and clear comment threads. Name the document management systems, collaboration tools, and style guides you've used so hiring managers can picture you functioning independently on a distributed team.
Target distributed clinical and regulatory teams
Remote medical writer roles concentrate at companies whose regulatory affairs or clinical operations are already distributed, not at firms transitioning reluctantly to remote work. Look for postings that mention distributed teams, asynchronous review cycles, or remote-first infrastructure in the role description.
Remote Medical Writer Jobs: Frequently Asked Questions
How do I get a remote medical writer job?
Target companies with distributed medical affairs, regulatory, or clinical teams, since those structures are built for remote medical writers. Remote employers screen heavily for self-direction, clear asynchronous written communication, and familiarity with tools like document management systems and shared style guides. A portfolio of regulatory documents, clinical study reports, or patient education materials gives you a concrete edge over candidates who can only describe their work.
Which companies hire remote medical writers?
Companies hiring remote medical writers right now include Veristat, サイネオス・ヘルス, and Precision Medicine, based on current remote listings on Migrate Mate as of September 2026. Remote medical writer roles concentrate at remote-first contract research organizations, specialty pharma firms, and digital health companies that run distributed regulatory and clinical writing teams.
Can you get a remote medical writer job with no experience?
Yes, but remote entry-level medical writer roles are harder to land because you're expected to work independently from day one without in-office support. Remote-first content agencies, medical communications firms, and digital health startups are more likely to consider entry-level candidates. A writing portfolio, completed coursework in life sciences or regulatory writing, and demonstrated ability to manage your own workflow can substitute for direct experience.
Do you need a degree for remote medical writer jobs?
Usually, but the field is more interested in your subject-matter knowledge and writing quality than your specific credential. Remote employers weigh a portfolio of clinical, regulatory, or scientific writing heavily alongside any formal background. Strong candidates show published or project-based work in life sciences writing, even when they don't hold an advanced degree.
Which industries hire the most remote medical writers?
Most remote medical writer openings sit in Biotechnology & Pharmaceuticals, Science & Research, and Healthcare & Medical Services, per current remote listings on Migrate Mate as of September 2026. Those sectors hire medical writers remotely because their regulatory, clinical, and communications teams are already built around distributed workflows and asynchronous collaboration.
See All 44 Remote Medical Writer Jobs
Find roles that match your experience and apply in just a few clicks.
Find Remote Medical Writer Jobs