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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 ...

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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 ...

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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 ...

twentysix

Medical Writer

Manhattan, NY · On-site

Trains/mentors junior writers on writing and company processes Qualifications and skills * You should bring a strong scientific background with a degree in a scientific or medical discipline (post ...

Adecco

Sr Med Writer

Morrisville, NC · Remote

$72.90 - $81/hr

Mentor and train junior medical writers on document development, regulatory requirements, processes, and therapeutic area knowledge. * Ensure documents meet applicable quality standards, regulatory ...

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 ...

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How much do junior medical writer jobs pay per hour?

As of Sep 14, 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 is a junior medical writer?

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 a junior medical writer do?

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.

What are the key skills and qualifications needed to thrive as a junior medical writer?

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.

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Junior Medical Writer jobs near you
Infographic showing various Junior Medical Writer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $63,608 per year, or $30.6 per hour.

[Voronoi, Inc.] Medical Writer (Hybrid Work)

Cambridge, MA • On-site

VORONOI, Inc.
See more jobs at VORONOI, Inc.external

Other

Posted 27 days ago

Job description

[Voronoi, Inc.] Medical Writer (Hybrid Work)

Medical Writer - Oncology Clinical Trials

Location: minimum 2 days onsite in Waltham, MA office Cambridge / Greater Boston

Position Summary:

We are seeking an experienced Medical Writer with a strong background in oncology clinical trials to join our growing company. The ideal candidate will have a deep understanding of oncology therapeutic areas and a proven track record of preparing high-quality regulatory and scientific documents in support of clinical development programs.

Key Responsibilities:
  • Develop, write, and edit clinical and regulatory documents related to oncology clinical trials, including but not limited to:
  • Clinical study protocols and amendments
  • Investigator brochures
  • Clinical study reports (CSRs)
  • Informed consent forms
  • Briefing documents
  • Clinical sections of INDs, NDAs, BLAs, and other regulatory submissions
  • Collaborate with cross-functional teams including Clinical Development, Regulatory Affairs, Biostatistics, Data Management, and Safety teams to ensure content accuracy and consistency
  • Interpret and synthesize complex clinical and scientific data into clear, concise, and scientifically sound documents
  • Ensure all documents comply with ICH guidelines, regulatory requirements, and internal SOPs
  • Participate in strategic planning and document timelines
  • Mentor junior medical writers or contractors as needed
  • Stay current with therapeutic area developments, industry trends, and regulatory guidance
Qualifications:
  • Advanced degree (PhD, PharmD, MD, or MSc) in life sciences, medicine, or a related field
  • Minimum 5 years of medical writing experience, with at least 3 years focused on oncology clinical trials
  • In-depth understanding of oncology disease areas and clinical endpoints
  • Extensive experience in authoring documents for Phase I–III oncology trials and regulatory submissions
  • Strong knowledge of ICH-GCP, FDA/EMA guidelines, and clinical trial processes
  • Excellent written and verbal communication skills
  • High attention to detail, strong analytical skills, and ability to manage multiple projects under tight deadlines
  • Proficiency with document management systems and MS Office Suite; experience with templates and style guides
Preferred Qualifications:
  • Experience working in a CRO, biotech, or pharmaceutical company
  • Familiarity with submission processes (eCTD) and regulatory publishing
  • Membership in professional organizations such as AMWA or EMWA is preferred
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