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Animal Study Director Jobs (NOW HIRING)

Altasciences

Animal Research Technician

Olyphant, PA · On-site

$16.25 - $22.25/hr

About the Role As an Animal Research Tech at Altasciences, you will perform technical procedures ... Support study supervisor(s) and study director(s) by performing and assisting with sample and data ...

Altasciences

Animal Research Technician

Olyphant, PA · On-site

$16.25 - $22.25/hr

About the Role As an Animal Research Tech at Altasciences, you will perform technical procedures ... Support study supervisor(s) and study director(s) by performing and assisting with sample and data ...

Bimeda

Cattleman

San Angelo, TX · On-site

Administer vaccines, challenge inoculations, and treatments according to study protocols study director supervision * Monitor animal health and clinical signs before and after vaccination or ...

Pharmatech Associates

$125 - $150/hr

The successful candidate will be comfortable working directly with animal study records, laboratory ... Direct experience auditing nonclinical facilities and studies to support pharmaceutical or ...

Altasciences

Animal Research Technician

Olyphant, PA · On-site

$16.25 - $22.25/hr

About the Role As an Animal Research Tech at Altasciences, you will perform technical procedures ... Support study supervisor(s) and study director(s) by performing and assisting with sample and data ...

Bimeda Inc.

Cattleman

San Angelo, TX · On-site

... study director supervision Monitor animal health and clinical signs before and after vaccination or challenge, recording observations accurately Collect biological samples (blood, serum, tissue ...

Altasciences

Animal Research Technician

Olyphant, PA

$16.25 - $22.25/hr

About the Role As an Animal Research Tech at Altasciences, you will perform technical procedures ... Support study supervisor(s) and study director(s) by performing and assisting with sample and data ...

Bimeda Inc.

Cattleman

San Angelo, TX · On-site

... study director supervision • Monitor animal health and clinical signs before and after vaccination or challenge, recording observations accurately • Collect biological samples (blood, serum ...

Corteva Agriscience

Study Coordinator

Newark, DE · On-site

... animal welfare, and continuous improvement. The Team Lead will help translate study plans into ... Coordinate with Planning & Management, Study Directors, PIs, and Technical Leads to align facility ...

Corteva Agriscience

Study Coordinator

Newark, DE · On-site

... animal welfare, and continuous improvement. The Team Lead will help translate study plans into ... Coordinate with Planning & Management, Study Directors, PIs, and Technical Leads to align facility ...

Integrated Resources INC

Animal Technician

Rockville, MD · On-site

... Study Director PURPOSE OF THE POSITION The Laboratory Assistant will perform a wide variety of ... Prepare animal carcasses for incineration Operate and maintain the cage and rack washing equipment ...

Frontage Laboratories

Vivarium Technician

Exton, PA · On-site

$15.25 - $20.50/hr

... Study Director Position Summary: We are seeking a reliable and detail-oriented Vivarium Technician to support in vivo studies in the DMPK department. The role involves routine animal care, assisting ...

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Animal Study Director information

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$45K

$128.4K

$232.5K

How much do animal study director jobs pay per year?

As of Sep 9, 2026, the average yearly pay for animal study director in the United States is $128,367.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $188,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Animal Study Director jobs?

For Animal Study Director jobs, the most frequently searched job titles are:

Infographic showing various Animal Study Director job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $128,367 per year, or $61.7 per hour.

GLP Auditor, Part 58, Animal Studies

Chicago, IL • On-site

Pharmatech Associates
1 - 10 employees
Learn more about Pharmatech Associatesexternal

$125 - $150/hr

Other

Posted 9 days ago

Job description

Pharmatech is proud to be an equal opportunity employer. Together we are committed to fostering an environment that is professional, inclusive and diverse. Explore the exciting opportunities currently available in the US and around the world.

Pharmatech Associates is seeking an experienced GLP Auditor, Contract/Project Consultant to support upcoming audits for our clients conducting regulated nonclinical research and animal studies

Position Overview

The GLP Auditor will provide independent assessment of contract GLP laboratories and their associated work as part of supplier oversight processes. The role requires the ability to assess not only whether procedures are followed, but also whether the resulting data can be relied upon, reconstructed, and supported by appropriate documentation. The successful candidate will be comfortable working directly with animal study records, laboratory data, protocols, raw data, computerized systems, equipment, facilities, and final reports, while applying the requirements of 21 CFR Part 58 and applicable regulatory expectations.

Key Responsibilities
  • Assess compliance with 21 CFR Part 58 principles, study protocols, SOPs, and applicable regulatory requirements.
  • Assess the effectiveness of the facilities QAU including study oversight.
  • Assess the adequacy of controls surrounding analytical methods, method validation, laboratory procedures, system suitability, and test results, as applicable.
  • Examine the qualification, calibration, maintenance, and operational status of laboratory and study equipment.
  • Evaluate computerized systems and electronic data environments, including validation status, user access, audit trails, data controls, and record retention.
  • Assess animal research environments, including animal identification, housing, care, environmental controls, facility practices, and associated documentation.
  • Prepare audit agendas and comprehensive audit reports that clearly distinguish regulatory findings, quality risks, supporting evidence, and potential impact on study integrity.
  • Review proposed remediation and CAPA plans, assess root-cause considerations, and verify that corrective actions are appropriately implemented and effective.
  • Provide practical recommendations regarding SOPs, processes, training, documentation practices, and quality controls where improvements are needed.
  • May be required to perform study audits as part of our client’s non-clinical study oversight.
Required Qualifications
  • At least 5 years of experience in GLP Quality Assurance, nonclinical research, or regulated auditing.
  • Must be able to travel to perform audits.
  • Demonstrated working knowledge of 21 CFR Part 58 requirements.
  • Direct experience auditing nonclinical facilities and studies to support pharmaceutical or biopharmaceutical product development.
  • Experience performing study audits, critical-phase audits, facility assessments, and/or external partner audits.
  • Ability to independently assess study documentation, raw data, source records, protocols, deviations, and final reports.
  • Understanding of data integrity principles, including ALCOA+ expectations, and their practical application to GLP records.
  • Strong technical writing skills and the ability to communicate audit conclusions clearly and objectively.

Pharmatech Associates, Inc. provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law.

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