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Temporary Regulatory Writing Jobs (NOW HIRING)

THE OPPORTUNITY Vir Biotechnology is looking for a Senior Regulatory Writer (Temporary) who will ... This Person will report to the Senior Director, Regulatory Writing. WHAT YOU'LL DO * Craft clear ...

THE OPPORTUNITY Vir Biotechnology is looking for a Senior Regulatory Writer (Temporary) who will ... This Person will report to the Senior Director, Regulatory Writing. WHAT YOU'LL DO * Craft clear ...

Regulatory Specialist

Erlanger, KY · On-site

$70K - $81K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Contract/Temporary. - Location: Erlanger, KY. Equal Opportunity Employer / Disabled / Protected ... Excellent written and verbal communication skills, including the ability to explain regulatory ...

A successful candidate will be able to write at a professional level and able to train client ... temporary in-plant positions. * Prepare project documentation, business presentations, and ...

A successful candidate will be able to write at a professional level and able to train client ... temporary in-plant positions. * Prepare project documentation, business presentations, and ...

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Senior Manager, Regulatory Compliance - Payments & Money Movement-TEMP

San Francisco, CA · On-site

$187K - $257K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

FULL-TIME TEMPORARY POSITION | HYBRID | CONFIDENTIAL SEARCH Confidential Search Solutions (CSS) is ... Excellent regulatory research, analytical, written communication, and documentation skills.

Posted today

Regulatory Specialist

Westlake, OH · On-site

$23 - $26/hr

  • Medical

  • Dental

Medical / Dental Insurance * $23/hr - $26/hr Employment Type & Shifts * Full Time * Temp to Hire ... Strong written and verbal communication skills * Excellent organizational and time management ...

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Senior Manager, Regulatory Compliance - Payments & Money Movement-TEMP

New York, NY · On-site

$187K - $250K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

FULL-TIME TEMPORARY POSITION | HYBRID | CONFIDENTIAL SEARCH Confidential Search Solutions (CSS) is ... Excellent regulatory research, analytical, written communication, and documentation skills.

Posted today

Regulatory Coordinator

Bohemia, NY · On-site

$65K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Work through regulatory changes, temporary deviations, and permanent product modifications, and ... Excellent written and verbal communication skills. * Proficiency with Microsoft Office Suite We ...

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Temporary Regulatory Writing information

See salary details

$15

$34

$145

How much do temporary regulatory writing jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for temporary regulatory writing in the United States is $34.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $26.20 per hour, depending on experience, location, and employer.

What are the most commonly searched types of Regulatory Writing jobs?

The most popular types of Regulatory Writing jobs are:

Infographic showing various Temporary Regulatory Writing job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 86% Full Time, 9% Part Time, and 3% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.

Senior Regulatory Writer (Temporary)

Vir Biotechnology

Remote

$130 - $170/hr

Temporary

Re-posted 25 days ago


Job description

THE OPPORTUNITY

Vir Biotechnology is looking for a Senior Regulatory Writer (Temporary) who will support all aspects of regulatory submissions writing needs. You will collaborate with senior management and other leads to support consistent documents/messaging within and across programs.  

This Person will report to the Senior Director, Regulatory Writing.

WHAT YOU'LL DO
  • Craft clear, accurate, and compliant documents required for regulatory submissions to global health authorities including but not limited to FDA and EMA
  • Write and edit a wide range of regulatory documents, including but not limited to: Clinical trial protocols and amendments, Investigator Brochures (IBs), Clinical Study Reports (CSRs), briefing packages, and components of regulatory submission dossiers (eg, NDA, IND, MAA) such as Module 2 and 5 summary documents (eg, SCS, SCE, ISS, etc)
  • Ensure that all written materials strictly adhere to regulatory guidelines, industry standards, and internal quality standards
  • Analyze complex scientific and medical information, including clinical trial data, translating it into clear, concise, and accurate language understandable by both technical and non-technical audiences
  • Work closely with cross-functional teams (eg, clinical research and operations, biostatistics, regulatory affairs, pharmacology, safety, etc) to ensure comprehensive and accurate document content
  • Manage writing projects from planning and coordination to submission, including establishing timelines and tracking progress
  • Provide teams with guidance about best practices and industry standards, offer solutions to authoring hurdles, support interaction and understanding across functional areas
WHO YOU ARE AND WHAT YOU BRING
  • Bachelor's degree  and 7 to 10+ years of industry experience required, advanced degree in science or medical field is a plus
  • Experience with most of the more common regulatory documents such as CSRs, IBs, DSURs, protocols, and clinical modules
  • Involvement with marketing applications (INDs, BLAs, NDAs, MAAs, or equivalents), preferably including responses to questions, 120-day safety updates, or other post-submission activities
  • Expert understanding of eCTD structure and the clinical development process, and in-depth knowledge of document-related ICH guidelines and GxPs
  • At least 8 years of experience as a regulatory writer in biotechnology or equivalent
#LI-AS1
#LI-Remote 

WHO WE ARE AND WHAT WE OFFER

The expected hourly range for this position is $130.00 to $170.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.