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Remote Medical Writing Consultant Jobs (NOW HIRING)

WORK LOCATION: The MWS Consultant I position is eligible for remote work based on company ... Strong foundation in medical writing, regulatory writing, and interpretation of scientific content.

Remote Medical Assistant

Ocala, FL · Remote

$16.50 - $21.25/hr

, remote Position: Remote Medical Assistant Company Overview: Absolute Elder Care is a leading ... Your responsibilities will include conducting virtual consultations, assisting with medication ...

Vaxcyte is seeking a Director, Clinical Medical Writing to drive and shape the medical writing ... San Carlos, CA or Remote Based Work Arrangement (may be adjusted based on business needs, job ...

Remote Medical Coder

$19.25 - $24.25/hr

We are seeking an experienced Medical Coder to join our healthcare consulting practice. The role is fully remote within the US. We are proud of our national presence, and excited to offer great ...

Medical Writing III

$137K - $167K/yr

Demonstrated expertise in medical and scientific writing principles and practices. Additional ... Remote Travel: May include some [domestic/international] travel Relocation Assistance: May be ...

... by consultants, contractors and vendors • Represent Medical Writing on multiple early phase project teams or on specific late phase project teams and collaborate with the Director of Medical ...

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Remote Medical Writing Consultant information

See salary details

$31K

$148.2K

$399K

How much do remote medical writing consultant jobs pay per year?

As of Jul 21, 2026, the average yearly pay for remote medical writing consultant in the United States is $148,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $97,500.00 and $181,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Medical Writing Consultant vs Remote Medical Writer?

AspectRemote Medical Writing ConsultantRemote Medical Writer
CredentialsTypically requires advanced degrees (e.g., MD, PhD, PharmD) and industry certificationsOften requires a degree in life sciences or related field; certifications are a plus
Work EnvironmentConsults with clients, provides strategic guidance, and reviews documentsPrepares, writes, and edits scientific and regulatory documents
Employer & Industry UsageConsulting firms, pharmaceutical companies, CROsPharmaceutical, biotech, and healthcare companies

Remote Medical Writing Consultants focus on providing expert advice, strategic input, and review services, often working on complex projects. Remote Medical Writers primarily produce and edit scientific and regulatory documents. Both roles require strong scientific knowledge, but the consultant role emphasizes strategic oversight and client interaction, while the writer role centers on document creation and editing.

More about Remote Medical Writing Consultant jobs
What cities are hiring for Remote Medical Writing Consultant jobs? Cities with the most Remote Medical Writing Consultant job openings:
What are the most commonly searched types of Medical Writing Consultant jobs? The most popular types of Medical Writing Consultant jobs are:
What states have the most Remote Medical Writing Consultant jobs? States with the most job openings for Remote Medical Writing Consultant jobs include:
Infographic showing various Remote Medical Writing Consultant job openings in the United States as of July 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% Remote job distribution, with an average salary of $148,159 per year, or $71.2 per hour.

Medical Writing Manager/Senior Manager - USA

Trilogy Writing and Consulting

Durham, NC • Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Job description

Salary:

Trilogy Writing & Consulting, anIndegenecompany,is currently looking to hireaMedical WritingManager/Senior Manager, reporting directly to the Director of Medical Writing,to support our growing company in producing regulatory documentation for the international pharmaceutical industry. At Trilogy, you will play a pivotal role in delivering comprehensive services to our clients that extend beyond writing. Our writers are integral members of clinical development teams supporting the writing andcoordinationof successful documentation across a broad spectrum of therapeutic areas. As our company continues to expand, there is room to develop withusand your ideas will form our future together. For further insight into who we are and what we do, please explore our website (www.trilogywriting.com).

Applicants must live in the USA and be authorized to work for any employer in the USA (we are unable to sponsor or take over sponsorship of an employment visa at this time); may work either fully remotely or a hybrid schedule (in office/remote) from our Durham, NC, USA office.

Job Overview:

As aMedical Writing Manager/Senior Manager, you will:

  • Provide line managementofa group ofmedicalwriters.
  • Provideresource oversightand guidance on a weekly basis.
  • Overseeprofessional development includingregular (i.e.quarterly) meetings with all members of the honeycomb.
  • Conduct annual and ad-hoc performance reviews for all members of the honeycomb.
  • Overseeeach employees timeandutilization.
  • Regularly reinforce the companys values and purpose tomaintaina sense of shared values, purpose, mission, and vision
  • Participate in Trilogy management-levelactivities.
  • Participate inbusiness development activities such as giving talks or workshops on behalf of Trilogy,participatingin management meetings to discuss strategic developments for the company,orrepresentingTrilogy at meetings withclients.
  • In addition,continue writing on client projects but have a reduced writing workload to accommodate these management activities.

Required experience and qualifications (professional skills) for this role:

  • Experience managing a team of medical writers inaline-management functionfor a minimum of 2 years.
  • A minimum of8years of medical regulatory writing experiencein a pharmaceutical, biotech, or CRO environment.
  • Demonstrated abilityand experience as a Lead Medical Writer on multiple types of regulatory documents/writing projects, including complex, multiple-document projectswith global, multinational teamssuch as submission dossiers or responses to regulatory authorities.
  • Experience in managementand coordination ofproject-level activities, including oversight of resources, otherwritersand QC, as well asuse ofsystematic methods to plan and perform tasks and coordinate people.
  • Experience with cost/benefit analyses for decision making (e.g.regardingresource assignment, conflict resolution, etc.)
  • Excellent interpersonal skills includingabilitytoguide andinfluence others internally and/or externally, effective decision-makingability,and excellent written and oral communication skills.


Trilogy offers the following:

  • Competitive base salary (starting from$160,000USD;dependent onexperience level and the Companys compensation practices)
  • Annual bonusopportunity dependent on personal and company performance
  • A generous allowance of paid time off (vacation, holiday, illness).
  • Comprehensive benefit plansthatinclude medical, dental, vision, short- and long-term disability, life insurance with AD&D.
  • Retirement savings plan with company match
  • Full AMWA membership and annual conference attendance paid for by Trilogy
  • Continuous personal and professional development opportunities
  • Free weekly yoga sessions
  • Other fun and excitingevents toencourage team bonding and development


Indegene is an Equal Opportunity Employer committed to fostering a culture of inclusion, diversity, and respect. We do not discriminate against any individual on the basis of race,color, religion or belief, sex, sexual orientation, gender identity or expression, age, national or ethnic origin, disability, marital or parental status, or any other characteristic protected under applicable laws. All employment decisions, including recruitment, hiring, training, compensation, promotion, and separation, are made based on business needs, individual merit, and qualifications.


It is important toIndegeneto ensure the highest possible degree of protection for your personal data. All personal data collected and processed within the scope of an application for employment with Trilogy are protected against unauthorized access and manipulation by technical and organizational measures and are notforwardedto third parties.Your data will be collected for the purpose of filling employment opportunities offered by Trilogy Writing & Consulting GmbH in Germany or its subsidiaries Trilogy Writing & Consulting Ltd in the UK,Trilogy Writing & Consulting, LLC in Canada,and Trilogy Writing & Consulting, Inc. in the USA.Bysubmittingyour data with this application, you consent to its use for this purpose within Trilogy. You can revoke this consent at any time without needing to give a reason by informing us of your revocation under jobs@trilogywriting.com.In the event ofrevocation, we willdeleteyour personal dataimmediately.