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Trilogy

Senior/Principal Medical Writer - USA

Durham, NC · On-site +1

$120K - $159K/yr

... remote) from our Durham, NC, USA office. You willbe responsible for: * Preparinga variety of ... ICH, FDA, EMA) for clinical trial conduct, including document-specific guidance. * For Principal ...

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How much do remote fda jobs pay per year?

As of May 31, 2026, the average yearly pay for remote fda in Raleigh, NC is $85,679.00, according to ZipRecruiter salary data. Most workers in this role earn between $49,778.00 and $111,156.00 per year, depending on experience, location, and employer.

What is a Remote FDA job?

A Remote FDA job typically involves working for or with the U.S. Food and Drug Administration (FDA) from a remote location. These roles can include regulatory affairs, compliance, medical writing, research, and reviewing submissions for drug and medical device approvals. Remote FDA jobs require knowledge of FDA regulations, strong analytical skills, and experience in healthcare, pharmaceuticals, or related fields. They offer flexibility while maintaining high regulatory standards and ensuring public health and safety.

What are the key skills and qualifications needed to thrive in the Remote Fda position, and why are they important?

To excel as a Remote FDA Compliance Specialist, you need in-depth knowledge of FDA regulations, quality assurance procedures, and a background in life sciences or a related field. Proficiency in using compliance management systems, electronic document management tools, and relevant certifications such as RAC (Regulatory Affairs Certification) are often required. Exceptional attention to detail, self-motivation, and strong written and verbal communication skills are vital for remote collaboration and thorough documentation. These abilities ensure regulatory adherence, minimize compliance risks, and facilitate effective remote teamwork within the pharmaceutical or medical device industry.

What are the typical daily responsibilities of a Remote FDA Compliance Specialist?

A Remote FDA Compliance Specialist generally reviews and updates regulatory documents, conducts virtual audits, and monitors company practices for FDA compliance. They regularly collaborate with cross-functional teams, such as quality assurance, legal, and product development, to provide guidance on regulatory requirements and respond to compliance queries. Additionally, they prepare and submit necessary reports, maintain records for inspections, and stay current on evolving regulations. This remote structure allows flexibility but also demands excellent organization, communication, and self-discipline to ensure all deadlines and compliance standards are met.
More about Remote Fda jobs
What are the most commonly searched types of Fda jobs in Raleigh, NC? The most popular types of Fda jobs in Raleigh, NC are:
What are popular job titles related to Remote Fda jobs in Raleigh, NC? For Remote Fda jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Fda jobs in Raleigh, NC look for? The top searched job categories for Remote Fda jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Fda jobs? Cities near Raleigh, NC with the most Remote Fda job openings:
Remote Fda jobs near you
Infographic showing various Remote Fda job openings in Raleigh, NC as of May 2026, with employment types broken down into 88% Full Time, and 12% Contract. Highlights an 100% Remote job distribution, with an average salary of $85,679 per year, or $41.2 per hour.

Senior/Principal Medical Writer - USA

Trilogy Writing and Consulting

Durham, NC • Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 20 days ago

Job description

Salary:

Trilogy Writing & Consulting,anIndegeneCompany, ishiringSenior/Principal Medical Writers (USA) 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 and coordination of successful documentation across a broad spectrum of therapeutic areas. As our company continues to expand, there is room to develop with us, and 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).
If this excites you, then apply below.

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.

You willbe responsible for:

  • Preparinga variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications) as the lead writer in collaboration with members of client authoring teams and supported by other writers, asappropriate.
  • Ensuringthat all documents are produced according to agreed timelines,monitorand manage project budgets, adhere to relevant SOPs, and meet the requirements of Trilogy as well as the companys clients.
  • Providingdocument-specific advice to clients.
  • Overseeingand coordinatingother writers and QC specialistsassisting ondocuments under your responsibility.
  • Project managingthe timelines andreviewcycles of your documents.
  • Workingin the clients regulatory document management systems.


Your impact:

As a Senior/Principal Medical Writer, you will:

  • Function as a lead writer to prepare a variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications) in collaboration with members of client authoring teams and supported by other writers, asappropriate.
  • Ensure that all documents are produced according to agreed timelines,monitorand manage project budgets, adhere to relevant SOPs, and meet the requirements of Trilogy as well as the companys clients.
  • Be responsible forprovidingdocument-specific advice to clients.
  • Oversee and coordinate other writers and QC specialistsassistingwith documents under your responsibility.
  • Projectmanagethe timelines and review cycles of your documents.
  • Work in the clients regulatory document management systems.


Qualified applicants musthave:

  • A minimum of aBachelors degree in science/pharmacy (Ph.D. not necessary).
  • Fluent written and spoken English skills.
  • A minimum of 3-5 years of experience of actively writing regulatory documents; experience as a lead writer on CTD documents is required for Principal Medical Writer.
  • Must have worked as the lead writer on key regulatory document(s)such as:
    Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications.
  • For Principal Medical Writer, must have experience as the lead writer with multiple-document projects with global, multinational teams, including team management, project management, review management, and budget oversight.
  • Must be able to manage multiple projects simultaneously.
  • Experience interacting directly with clients or authors of the documents and coordinating review cycles, meetings, and project timelines.
  • Must have in-depth working knowledge of the relevant regulatory guidance (e.g.ICH, FDA, EMA) for clinical trial conduct, including document-specific guidance.
  • For Principal Medical Writer,Experience in multiple therapeutic areas to have confidence to work in these areas without lead-in time.
  • Competency in the use of document management systems and review tools.
  • Experience interacting directly with clients or authors ofthe documentsand coordinating review cycles, meetings, and project timelines.
  • For the Principal Medical Writer level,abilityand willingness to take on any project for which a Lead Writer is needed.
  • Competency in the use of document management systems and review tools.
  • An appreciation for a well-written document and an eye for details.
  • Excellent, proven interpersonal skills, and enjoy proactivelyparticipatingona team with diverse personalities.
  • Flexibility and the ability to stay focused under tight timelines.

Perks:

  • Competitive base salary (range:$120,000 to $159,000USD; the salary range is an estimate and may vary based on experience level, region, and the Companys compensation practices)
  • Annual bonus opportunity
  • A generous allowance of paid time off (vacation, holiday, birthday, illness).
  • Comprehensive benefitplans toinclude medical, dental, vision, disability, lifeinsurance with AD&D.
  • 401Kretirement 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 exciting eventsthatencourage team bonding and development


EQUAL OPPORTUNITY

Trilogy Writing & Consulting, an Indegene Company, is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminateon the basis ofrace, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidatesmeritand qualification.

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.