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Junior Medical Writing 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 ...

Prometrika LLC

Manager, Medical Writing

Cambridge, MA · On-site

$136K - $164K/yr

Manage and supervise junior medical writers and/or external contractors * Oversee and/or participate in the development/writing of: * Clinical Development Plans (CDPs) * Clinical study protocols and ...

Prometrika LLC

Senior Medical Writer

Cambridge, MA · On-site

$134K - $162K/yr

... Medical Writing departmental initiatives aligned with organizational strategic goals * Uphold, demonstrate and teach junior team members PROMETRIKA's Core Competencies * Assist with developing ...

Icon plc

Principal Medical Writer

Blue Bell, PA

Providing guidance on best practices for medical writing and ensuring adherence to regulatory requirements and internal standards * Mentoring and training junior medical writers, fostering a culture ...

ICON

Principal Medical Writer

Blue Bell, PA · On-site +1

Providing guidance on best practices for medical writing and ensuring adherence to regulatory requirements and internal standards * Mentoring and training junior medical writers, fostering a culture ...

Icon plc

Providing guidance on best practices for medical writing and ensuring adherence to regulatory requirements and internal standards * Mentoring and training junior medical writers, fostering a culture ...

Genmab A/S

Director, Medical Writing

Princeton, NJ · On-site +1

$198K - $297K/yr

Mentor new employees and consultants and serve as a role model for junior writers. * Guide medical writing staff during the planning and execution stages across all document types and regulatory ...

Genmab

Director, Medical Writing

Plainsboro, NJ

$198K - $297K/yr

Mentor new employees and consultants and serve as a role model for junior writers. * Guide medical writing staff during the planning and execution stages across all document types and regulatory ...

Envision Pharma Group

Medical Writer

$78K - $102K/yr

Advance your medical writing career with purpose and impact. Work shouldn't just be something we do ... fit for junior Medical Writers looking to expand their publications experience. We welcome ...

MJH Life Sciences

Principal Medical Writer

Cranbury, NJ · On-site

$95K - $105K/yr

This will require supplying accurate precise directives for each assignment, review and guidance in best practices of writing/editing, * Provide training and mentorship to junior Medical Writers and ...

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Junior Medical Writing information

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$12

$30

$58

How much do junior medical writing jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for junior medical writing 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 is a Junior Medical Writer?

A Junior Medical Writer is an entry-level professional who assists in creating scientific documents, such as clinical study reports, regulatory submissions, and medical publications. They work under the supervision of senior medical writers or project managers, ensuring the accuracy and clarity of medical information. Junior Medical Writers often collaborate with researchers, clinicians, and regulatory teams to gather data and present it in a clear, compliant manner. This role typically requires strong writing skills, a background in life sciences, and attention to detail.

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

To thrive as a Junior Medical Writer, you need a strong grasp of scientific and medical concepts, excellent written communication, and typically a life sciences degree. Familiarity with referencing software (like EndNote), Microsoft Office Suite, and guidelines such as ICH or AMA style is often required. Attention to detail, time management, and the ability to collaborate with multidisciplinary teams are valuable soft skills. These competencies ensure the production of accurate, compliant, and effective medical documents that support research, regulatory submissions, and healthcare communications.

What is the difference between Junior Medical Writing vs Medical Writing?

AspectJunior Medical WritingMedical Writing
Required CredentialsBachelor's degree, training in medical or life sciencesBachelor's or higher in life sciences, with experience or certification preferred
Work EnvironmentEntry-level, supporting senior writers, often in pharmaceutical or biotech companiesProfessional, independent or team-based, in healthcare, pharma, or CRO settings
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsSame as Junior Medical Writing, with broader scope and experience
Search & Comparison IntentUnderstanding entry-level roles in medical writingSeeking experienced medical writers or career progression

Junior Medical Writers typically have less experience and focus on supporting senior writers in creating clinical, regulatory, or marketing documents. Medical Writers are more experienced, often handling complex projects independently. The roles overlap in industry and credentials but differ mainly in experience level and scope of responsibilities.

What types of projects and documents are typically assigned to a Junior Medical Writer, and how are these prioritized within a medical writing team?

As a Junior Medical Writer, you will often work on tasks such as drafting clinical study protocols, patient information sheets, regulatory submission documents, and literature summaries. These projects are usually assigned based on team deadlines, your prior experience, and the complexity of each document. Junior writers often begin with supporting sections or less complex tasks, receiving guidance from senior writers and project managers. Collaboration and regular feedback are key, helping you build expertise while ensuring high-quality deliverables that meet regulatory and scientific standards.
More about Junior Medical Writing jobs
What cities are hiring for Junior Medical Writing jobs? Cities with the most Junior Medical Writing job openings:
What are the most commonly searched types of Medical Writing jobs? The most popular types of Medical Writing jobs are:
What states have the most Junior Medical Writing jobs? States with the most job openings for Junior Medical Writing jobs include:
What job categories do people searching Junior Medical Writing jobs look for? The top searched job categories for Junior Medical Writing jobs are:
Junior Medical Writing jobs near you
Infographic showing various Junior Medical Writing job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 89% Full Time, and 9% Contract. 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 19 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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