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Full Time Remote Medical Writer Jobs (NOW HIRING)

BeiGene, Inc.

Senior Principal Medical Writer

This position is also responsible for mentoring MWs (full-time employees and/or contractors/vendors ... medical writing communities). Supervisory Responsibilities: * None. Education Required: * An ...

CareHarmony

Remote - Medical Receptionist

$14.50/hr

CareHarmony has an immediate opening for a Remote Medical Receptionist with a solid phone presence ... Excellent written and verbal communication skills * Excellent interpersonal and customer service ...

Scribe-X

Remote Medical Scribe

Winston Salem, NC · Remote

$14 - $17/hr

Excellent verbal and written English skills * Strong computer skills with the ability to learn and ... If no college degree, 1+ years of full time work experience as a scribe * Most assignments require ...

Scribe-X

Remote Medical Scribe

Boise, ID · Remote

$14 - $17/hr

Excellent verbal and written English skills * Strong computer skills with the ability to learn and ... If no college degree, 1+ years of full time work experience as a scribe * Most assignments require ...

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Full Time Remote Medical Writer information

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$14

$38

$57

How much do full time remote medical writer jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for full time remote medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is the difference between Full Time Remote Medical Writer vs Medical Communications Specialist?

AspectFull Time Remote Medical WriterMedical Communications Specialist
CredentialsTypically requires a degree in life sciences, healthcare, or related field; certifications like AMWA or EMWA are commonSimilar credentials; often holds advanced degrees and certifications in medical writing or communication
Work EnvironmentPrimarily remote, working independently or with teams on scientific documentsCan be remote or in-office, involved in creating and managing medical communication materials
Industry UsageUsed across pharmaceutical, biotech, and healthcare industries for document preparationCommon in pharmaceutical marketing, medical education, and scientific publication sectors

While both roles require scientific expertise and similar credentials, Full Time Remote Medical Writers focus on creating scientific documents remotely, whereas Medical Communications Specialists often handle broader communication strategies, sometimes in a more collaborative or client-facing setting.

Can you work from home as a medical writer?

Full-time remote medical writers can work from home, as many companies and organizations hire for remote positions that involve writing scientific content, regulatory documents, or medical communications. Successful remote medical writers typically have strong writing skills, relevant certifications, and proficiency with tools like reference management software and collaboration platforms. Flexibility in schedule and self-discipline are also important for remote work in this field.

How can I make $70,000 a year working from home?

A full-time remote medical writer can earn $70,000 or more annually by gaining relevant medical or scientific writing skills, obtaining certifications, and building a strong portfolio. Consistently producing high-quality content, meeting deadlines, and working with reputable clients or organizations can help achieve this income level.

How to make $100,000 a year working from home?

A full-time remote medical writer can earn $100,000 annually by gaining specialized knowledge in a high-demand medical field, building a strong portfolio, and working for reputable organizations or freelance clients. Developing skills in scientific writing, obtaining relevant certifications, and using professional tools like reference management software can enhance earning potential. Consistent quality work and expanding your client base are key to reaching this income level.

How can I make 2000 a week working from home?

A full-time remote medical writer can earn $2,000 or more weekly by producing high-quality scientific or medical content, often charging per project or word. Building expertise, obtaining relevant certifications, and working with multiple clients or agencies can increase earning potential. Consistent, efficient work and strong research skills are essential for reaching this income level.
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What cities are hiring for Full Time Remote Medical Writer jobs? Cities with the most Full Time Remote Medical Writer job openings:
What are the most commonly searched types of Remote Medical Writer jobs? The most popular types of Remote Medical Writer jobs are:
What states have the most Full Time Remote Medical Writer jobs? States with the most job openings for Full Time Remote Medical Writer jobs include:
What job categories do people searching Full Time Remote Medical Writer jobs look for? The top searched job categories for Full Time Remote Medical Writer jobs are:
Full Time Remote Medical Writer jobs near you
Infographic showing various Full Time Remote Medical Writer job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 98% Full Time, and 1% Part Time. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.
Senior Principal Medical Writer

Senior Principal Medical Writer

BeiGene, Inc.

Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
This position is responsible for providing expertise to support the development of high-quality, fit-for-purpose clinical and regulatory documents to facilitate speed of information during development, submission, approval, and life-cycle management of products in BeiGene pipeline. The clinical and regulatory documents include, but are not limited to, clinical study protocols, investigator brochures, clinical study reports, regulatory briefing documents, clinical modules of INDs, NDAs, BLAs, MAAs and other regulatory submissions, and other types of clinical and regulatory documents within the working scope of global medical writing. This position is also responsible for mentoring MWs (full-time employees and/or contractors/vendors) as needed.
Essential Functions of the Job:
Document Writing:
  • Manages the assigned writing tasks and ensures that the documents adhere to relevant regulatory guideline(s), as well as BeiGene SOP/WI(s), template(s), and style guide.

  • Be able to manage multiple documents at the same time, including the complex documents (eg, those with complex content, urgent timeline, or external collaboration). Proactively leads direction and strategy setting (including critically analyzing, synthesizing, and presenting complex information) for document development in collaboration with study team(s), and be able to guide other MWs.

  • Leads part of the creation of document writing template/guidance for all document types within the working scope. Leads the maintenance of document writing template/guidance for all document types within the working scope.

Project /Program Management:
  • Navigates through uncertainties to develop and manage timeline of individual documents and multiple documents (supported by different MWs in one project, eg, works as the MW filing lead for an NDA/BLA/MAA submission), including those for complex projects. Be able to guide other MWs.

  • Proactively identifies the questions/issues/potential risks that require departmental discussion or team discussion. Proactively identifies the potential risks and makes a mitigation plan. Resolves problems efficiently and skillfully. Be able to guide other MWs in these areas.

  • Builds strong and in-depth relationship with study team(s) and program team(s) (eg, works as the MW program lead).

  • Understands the role of own documents within the larger dossier and voices out any impact on upstream and downstream processes. Be able to guide other MWs and provide suggestions.

Process/Tool Establishment and Optimization:
  • Proactively identifies needs for process/tool optimization and establishment, and proposes solutions.

  • Leads departmental process/tool optimization. Leads (part of) departmental process/tool establishment.

  • Leads part of cross-functional process/tool optimization. Contributes to cross-function process/tool establishment.

  • Contributes to cross-company process/tool optimization.

Training and Mentoring:
  • Leads (part of) the development of new training programs. Provides instructions/trainings (content-wise/process-wise) to other MWs.

  • Provides systematic technical and operational mentorship to MWs (full-time employees and/or contractors/vendors).

Influence:
  • Understands the global MW scope and works to guide study team(s) and program team(s) within the defined scope and responsibility following established processes.

  • Provides topic sharing on regulatory writing and related knowledge within the department and to cross-functional stakeholders.

  • Provides topic sharing on regulatory writing and related knowledge across companies (eg, meetings of DIA and medical writing communities).

Supervisory Responsibilities:
  • None.

Education Required:
  • An advanced degree (MS/PhD/PharmD/MD) in life science, pharmacy, medical, or health-related science is preferred.

  • BS with a minimum of 7 years of regulatory document writing (or equivalent) experience, master's with 5+ or PhD/PharmD/MD with a minimum of 3+ years of regulatory document writing (or equivalent) experience.

Computer Skills:
Technical expertise in Microsoft Word, Adobe Acrobat, and electronic document management systems; proficiency in Microsoft Outlook, Excel, and PowerPoint, etc.
Travel:
On occasion, as needed.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $137,100.00 - $182,100.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
BeiGene logo

About BeiGene

Sourced by ZipRecruiter

BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

Social media

Twitter

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