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Remote Junior Medical Writer Jobs (NOW HIRING)

Mentors junior and contract medical writers on both document and timeline management. Required Skills, Experience and Education: * 8-11 years of clinical regulatory writing experience within one or ...

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

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Remote Junior Medical Writer information

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$12

$30

$58

How much do remote junior medical writer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for remote 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 the difference between Remote Junior Medical Writer vs Remote Medical Writer?

AspectRemote Junior Medical WriterRemote Medical Writer
Required CredentialsBachelor's degree in life sciences or related field; some roles may prefer or require a relevant certificationBachelor's or higher in life sciences; often requires or prefers additional certifications or experience
Work EnvironmentEntry-level, collaborative, often supervised; remote or hybrid options commonMore autonomous, experienced; primarily remote, with potential for client interaction
Employer & Industry UsagePharmaceutical, biotech, medical communications agencies; entry-level rolesPharmaceutical companies, CROs, medical communication agencies; mid-level to senior roles

The main difference between a Remote Junior Medical Writer and a Remote Medical Writer lies in experience and responsibility. Junior writers are typically entry-level, focusing on learning and supporting senior staff, while Medical Writers have more experience and handle more complex projects independently. Both roles often work remotely within the healthcare and pharmaceutical industries, but the level of autonomy and expectations differ.

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What cities are hiring for Remote Junior Medical Writer jobs?

Cities with the most Remote Junior Medical Writer job openings:

What are the most commonly searched types of Remote Medical Writer jobs?

The most popular types of Remote Medical Writer jobs are:

What states have the most Remote Junior Medical Writer jobs?

States with the most job openings for Remote Junior Medical Writer jobs include:

Infographic showing various Remote Junior Medical Writer job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% Remote job distribution, with an average salary of $63,608 per year, or $30.6 per hour.

Full-time

Re-posted 14 days ago


Job description

The Opportunity:
Revolution Medicines is seeking a motivated individual with a clinical regulatory writing background to play a critical role in the successful preparation of high-quality, submission-ready clinical research documents. This role is an individual contributor with team leadership responsibilities, reporting to the Executive Director, Medical Writing.

This position is responsible for drafting and managing the content and reviews of clinical regulatory documents for Revolution Medicines products in various drug development phases.

  • Serves as medical writing lead on complex clinical regulatory documents, including protocols, IBs, CSRs, briefing documents, periodic safety reports, risk management documents, and IND and NDA modules.

  • Assists in developing and maintaining document templates, department standard processes and work instructions, medical writer onboarding materials, and style guide.

  • Serves as primary medical writing contact for one or more clinical development programs.

  • Represents medical writing at cross-functional planning meetings.

  • Effectively communicates deliverables needed, the writing process, and timelines to team members.

  • Schedules document reviews and manage adjudication meetings.

  • Holds team members accountable to agreed-upon project dates.

  • Independently resolves document content issues and questions.

  • Ensure consistency, clarity, and accuracy both within and across documents.

  • Recognizes potential scheduling and resource conflicts across projects and provides recommendations to resolve.

  • Mentors junior and contract medical writers on both document and timeline management.

Required Skills, Experience and Education:

  • 8-11 years of clinical regulatory writing experience within one or more biopharmaceutical companies, including prior experience working as a medical writer for a BLA/NDA/MAA.

  • Advanced degree in clinical or life sciences, English, journalism, and/or communications.

  • Proficiency in Microsoft Word, including the use of MS Word styles and templates.

  • Familiarity with AMA style.

  • Ability to successfully manage and prioritize writing projects with competing deadlines, to foster collaborative cross-functional relationships, and to drive high-quality regulatory writing projects to successful submission.

  • Ability to work in a high-pressure environment with short deadlines while remaining calm, focused, professional, diplomatic, and positive.

Preferred Skills:

  • Experience with oncology therapeutics.

  • Familiarity with StartingPoint, EndNote, Veeva RIM, and Smartsheet.

  • Experience performing QC reviews of clinical regulatory documents. 

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