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Temporary Pharmacologist Jobs (NOW HIRING)

THE OPPORTUNITY Vir Biotechnology is looking for a Senior Regulatory Writer (Temporary) who will ... pharmacology, safety, etc) to ensure comprehensive and accurate document content * Manage writing ...

The Research Associate, Discovery Biology and Pharmacology is a 6+ months temporary role with a possibility of conversion to full-time in our Research division. The position is in a dynamic and ...

Lead optimization, in vitro preclinical studies and clinical pharmacokinetic analysis. * In-vivo ... Temporary Regular FLSA Status Exempt Organizational Group College Pharmacy Department PHARMACY ...

Pharmacist in Caballo, NM

Caballo, NM

$50.25 - $60.25/hr

... temporary license * Proven inpatient hospital pharmacy experience * Strong knowledge of medication order verification and pharmacokinetics * Ability to supervise and lead pharmacy support staff ...

... scientist for a temporary position (~6 months). Successful candidate will be able to work ... Design and execute large and complex in vivo studies to assess pharmacokinetic and pharmacodynamic ...

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How much do temporary pharmacologist jobs pay per year?

As of Aug 17, 2026, the average yearly pay for temporary pharmacologist in the United States is $127,248.00, according to ZipRecruiter salary data. Most workers in this role earn between $112,000.00 and $142,500.00 per year, depending on experience, location, and employer.

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States with the most job openings for Temporary Pharmacologist jobs include:

Senior Regulatory Writer (Temporary)

Vir Biotechnology

Remote

$130 - $170/hr

Temporary

Re-posted 24 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.