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Junior Medical Writer Jobs (NOW HIRING)

Medasource

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

This role requires advanced medical writing skills, deep knowledge of regulatory requirements, the ability to mentor junior writers, and strong interpersonal and presentation abilities. Candidates ...

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Principal Medical Writer

Blue Bell, PA

Mentoring and training junior medical writers, fostering a culture of excellence and professional growth * Staying current with industry trends and regulatory guidelines to inform writing practices ...

ICON

Principal Medical Writer

Blue Bell, PA · On-site +1

Mentoring and training junior medical writers, fostering a culture of excellence and professional growth * Staying current with industry trends and regulatory guidelines to inform writing practices ...

Icon plc

Mentoring and training junior medical writers, fostering a culture of excellence and professional growth * Staying current with industry trends and regulatory guidelines to inform writing practices ...

Prometrika LLC

Senior Medical Writer

Cambridge, MA · On-site

$134K - $162K/yr

Mentor and train junior medical writers and/or external contractors * Work with the sponsor's and/or PROMETRIKA's medical personnel and statisticians to develop/write clinical development plans ...

Envision Pharma Group

Medical Writer

$78K - $102K/yr

This opportunity provides clear growth potential for Associate Medical Writers seeking promotion, while also being an excellent fit for junior Medical Writers looking to expand their publications ...

Real Chemistry

Senior Medical Writer

Train and mentor more junior medical writers under the guidance of the Medical Director * Maintain full compliance with legal, regulatory, and corporate requirements as well as all applicable US laws ...

MJH Life Sciences

Principal Medical Writer

Cranbury, NJ · On-site

$95K - $105K/yr

Provide training and mentorship to junior Medical Writers and Editors, offering guidance on best practices in medical writing and editing. * Assist writers/editors on the team in workload ...

Syneoshealth

OR

Mentor more junior medical writing staff. Minimum Requirements and Competencies: * Bachelor's degree required. Advanced degree in a relevant scientific/clinical/regulatory field preferred. * At least ...

IQVIA

Senior Medical Writer

Durham, NC · On-site

Provides written and verbal feedback to junior staff, and to customers when appropriate. Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical ...

IQVIA, Inc.

Senior Medical Writer

Durham, NC · On-site

Provides written and verbal feedback to junior staff, and to customers when appropriate. Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical ...

IQVIA

Senior Medical Writer

Durham, NC

Provides written and verbal feedback to junior staff, and to customers when appropriate. Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical ...

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Junior Medical Writer information

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How much do junior medical writer jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for junior medical writer in the United States is $30.58, according to ZipRecruiter salary data. Most workers in this role earn between $22.84 and $30.77 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Junior Medical Writer position, and why are they important?

To thrive as a Junior Medical Writer, you need a background in life sciences or related fields, strong research skills, and excellent written communication abilities. Familiarity with referencing software (such as EndNote or Mendeley), Microsoft Office Suite, and basic understanding of medical writing guidelines like ICH or GPP is often required. Attention to detail, time management, adaptability, and the ability to accept feedback are valuable soft skills for this role. These capabilities ensure you can accurately and effectively convey complex medical information while meeting deadlines and collaborating in a team environment.

What is a Junior Medical Writer job?

A Junior Medical Writer is an entry-level professional responsible for creating clear, accurate, and well-structured medical content for various audiences, including healthcare professionals and patients. They work under the guidance of senior writers and medical experts to develop documents such as clinical trial reports, regulatory submissions, and educational materials. Strong research skills, attention to detail, and the ability to translate complex medical information into accessible content are essential for this role. Junior Medical Writers often collaborate with medical teams, regulatory authorities, and clients to ensure accuracy and compliance with industry standards.

What does the day-to-day routine look like for a Junior Medical Writer?

A Junior Medical Writer typically spends their days researching medical topics, drafting content such as clinical study reports, regulatory documents, or educational materials, and revising drafts based on feedback from senior writers or clients. Collaboration is frequent, as you’ll interact with medical professionals, editors, and project managers to ensure accuracy and compliance with industry standards. Many junior writers also participate in meetings to discuss project timelines and client requirements. Over time, you may take on more complex writing assignments and develop greater independence as you gain experience. This dynamic routine provides opportunities to learn from experienced colleagues and grow your medical writing expertise.

More about Junior Medical Writer jobs
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Junior Medical Writer jobs near you
Infographic showing various Junior Medical Writer job openings in the United States as of June 2026, with employment types broken down into 25% As Needed, and 75% Full Time. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $63,608 per year, or $30.6 per hour.
Lead Medical Writer

Lead Medical Writer

Medasource

Dublin, OH • On-site

$80 - $90/hr

Contractor

Posted 21 days ago

Job description

Lead Medical Writer
Remote (must be based in EST)
Compensation: $80-$90 per hour
Contract Length: 2 month Contract to Hire (40 hours/week)
Start Date: 7/1/26
ABOUT THE ROLE
Our client is a global healthcare services and products company providing pharmaceuticals, medical products, and supply chain solutions to hospitals, pharmacies, and healthcare providers. The organization plays a critical role in helping healthcare systems improve efficiency, reduce costs, and enhance patient care through integrated distribution and data-driven solutions. As a Lead Medical Writer on a 2-month remote contract, you will autonomously author and review a range of clinical regulatory documents, including CTD Module II summaries, Clinical Overviews, Clinical Study Reports (CSRs), and responses to health authority queries. You will contribute scientifically and strategically to submission teams, plan data analyses, review statistical analysis plans, and collaborate with cross-functional stakeholders such as Clinical Sciences, Clinical Pharmacology, Biometry, Drug Safety, Clinical Operations, CMC, and Regulatory Affairs. This role requires advanced medical writing skills, deep knowledge of regulatory requirements, the ability to mentor junior writers, and strong interpersonal and presentation abilities. Candidates must be available to work in the Eastern Standard Time zone.
WHAT YOU'LL DO
  • Autonomously write and review clinical regulatory documents, including CTD Module II summaries, Clinical Overviews, Clinical Study Reports (CSRs), and other regulatory submissions such as responses to health authority questions, briefing books, 120-day safety updates, pediatric investigational plans, and investigator brochures
  • Contribute scientifically and strategically to submission teams at the project and/or study team level, providing input on pooling strategy, content expertise, and guidance on regulatory requirements
  • Plan and review data analyses and presentations for CSRs; review statistical analysis plans and related documents
  • Collaborate effectively with cross-functional stakeholders, including Clinical Sciences, Clinical Pharmacology, Biometry, Drug Safety, Clinical Operations, CMC, and Regulatory Affairs
  • Work with in-house Documentation Specialists to produce high-quality final documents and ensure timely delivery
  • Mentor and develop junior medical writers, providing guidance and support as needed
  • Demonstrate advanced medical writing skills and maintain up-to-date knowledge of regulatory document requirements and guidelines
  • Work independently and as part of a team, managing multiple priorities and meeting challenging deadlines
  • Exhibit excellent interpersonal and presentation skills in all interactions
  • Maintain advanced proficiency in English for all written and verbal communications
WHAT YOU BRING
  • Advanced degree in life sciences (PhD, PharmD, MD, or MS preferred)
  • 5+ years of regulatory/medical writing experience in the pharmaceutical industry across several therapeutic areas
  • Proven ability to autonomously write and review clinical regulatory documents (e.g., CTD Module II summaries, CSRs, Clinical Overviews, Investigator brochures, and other regulatory submissions)
  • Strong knowledge of regulatory document requirements and guidelines
  • Experience contributing scientifically and strategically to submission teams
  • Ability to plan data analyses and review statistical analysis plans for CSRs
  • Excellent collaboration skills with cross-functional stakeholders
  • Well-developed medical writing skills with attention to quality and deadlines
  • Ability to mentor and develop junior medical writers
  • Ability to work independently and as part of a team
  • Strong interpersonal and presentation skills
  • Advanced level of English proficiency
  • Ability to work under pressure and meet challenging deadlines
  • Remote work capability with availability in Eastern Standard Time (EST)

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