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Full Time Senior Medical Writer Jobs (NOW HIRING)

Veristat

The Sr Medical Writer will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team.

Veristat

The Sr Medical Writer will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team.

Parexel

Senior Medical Writer - FSP

Parexel FSP has an exciting opportunity for a Medical Writer ! Key Accountabilities : Author Clinical Documents * Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and ...

MMS

Senior Medical Writer (Remote)

Zionsville, IN · On-site

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...

MMS

Senior Medical Writer (Remote)

Canton, MI · On-site

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...

MMS

Senior Medical Writer (Remote)

Philadelphia, PA · On-site

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...

Icon plc

The position includes all duties of a Senior Medical Writer, as well as leadership of regulatory approval application writing Your Profile: You will have solid experience in medical writing, with the ...

MMS

Senior Medical Writer (Remote)

Aurora, CO · On-site

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...

ICON

Principal Medical Writer

Blue Bell, PA · On-site +1

The position includes all duties of a Senior Medical Writer, as well as leadership of regulatory approval application writing Your Profile: You will have solid experience in medical writing, with the ...

MMS

Senior Medical Writer (Remote)

Miami, FL · On-site

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...

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Full Time Senior Medical Writer information

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$35K

$137.3K

$247.5K

How much do full time senior medical writer jobs pay per year?

As of Aug 10, 2026, the average yearly pay for full time senior medical writer in the United States is $137,286.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,000.00 and $166,000.00 per year, depending on experience, location, and employer.

Is there a demand for full time senior medical writers?

There is a strong and growing demand for full-time senior medical writers due to the increasing need for clear scientific communication in the healthcare and pharmaceutical industries. These roles often require expertise in medical terminology, regulatory guidelines, and proficiency with tools like reference management software. The demand is driven by ongoing clinical research, drug development, and regulatory submission processes.

Do full time senior medical writers make good money?

Full-time senior medical writers typically earn a competitive salary that reflects their experience, expertise, and the complexity of medical writing tasks. Salaries often range from $80,000 to over $150,000 annually, depending on the industry, location, and whether they work in pharmaceutical, biotech, or healthcare communications. They may also receive benefits such as bonuses, health insurance, and professional development opportunities.

How much do full time senior medical writers make in the US?

Full-time senior medical writers in the US typically earn between $100,000 and $150,000 annually, depending on experience, location, and employer. They often possess advanced degrees in life sciences and strong writing skills, with some roles offering additional benefits or bonuses.
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Full Time Senior Medical Writer jobs near you
Infographic showing various Full Time Senior Medical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $137,286 per year, or $66 per hour.

Senior Medical Writer - clinical focus

Veristat

Remote

Full-time

Medical, Retirement

Re-posted 8 days ago

Job description

Job Description:

Position overview

The Senior Medical Writer- Clinical Focus is a major contributor to document authorship for a variety of documents across different service lines. The Sr Medical Writer will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team. Veristat is looking for individuals looking to use their expertise in clinical regulatory writing to lead teams and help clients achieve their goals.

Make an Impact at Veristat!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

  • 105+ approved therapies for marketing applications prepared by Veristat
  • 480+ oncology projects in the past 5 years
  • 350+ rare disease projects delivered in the past 5 years
  • Flexible, inclusive culture - 70% remote workforce, 66% women-led teams

Learn more about our core valueshere!

What we offer

  • The estimated hiring range for this role is $116K-128K plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.
  • Benefits vary by location and may include:
  • Remote working
  • Flexible time off
  • Paid holidays
  • Medical insurance
  • Tuition reimbursement
  • Retirement plans

What we look for

  • Bachelor's degree or higher in a scientific discipline strongly preferred
  • 3+ years of regulatory writing experience or equivalent experience with clinical related documentation
  • Understand regulatory authority guidelines and requirements to be able to lead an internal project team and anticipate the effects that writing practice conventions can have on the final product when seeking health authority approval/acceptance
  • Experience in the development of submission-level documents (does not require functioning as a document lead)
  • Experience in the development of clinical documents such as Clinical Study Reports, Investigator Brochures, protocols, ISS, and/or ISE

Skills & Abilities:

  • Intermediate proficiency with Microsoft Word skills (editing tools, creating and modifying tables and inserting figures) and document management techniques
  • Strong understanding of the document creation process and of the drug development lifecycle
  • Able to synthesize data across multiple data sources and documents to create summary reports
  • Ability to conduct/lead a CRM and successfully lead a project team to consensus
  • Ability to use logical arguments to persuade others when presenting ideas and suggestions, but also respond positively to opposing views voiced by others
  • Develops professional relationships with clients as a way to further the business relationship and maintain current industry knowledge
  • Ability to identify and institutionalize work practices that are most effective in order to ensure consistency in performance

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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