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Study Director Primate Jobs (NOW HIRING)

RPM ReSearch

Study Director II

Corpus Christi, TX · On-site

$80K - $110K/yr

Study Director - Non-Human Primate Research Program Location: Corpus Christi, Texas Job Type: Full-Time About the Opportunity Are you an experienced Study Director with a passion for in-vivo research ...

Labcorp

Senior Primate Behavior Specialist

Greenfield, IN · On-site

$19 - $25.50/hr

Labcorp is seeking a Senior Primate Behaviorist to join our team in Greenfield, IN. Job ... Develop behavior management projects for study related procedures, collaborate with study directors ...

Labcorp

Senior Primate Behavior Specialist

Greenfield, IN · On-site

$19 - $25.50/hr

Labcorp is seeking a Senior Primate Behaviorist to join our team in Greenfield, IN. Job ... Develop behavior management projects for study related procedures, collaborate with study directors ...

Labcorp

Senior Primate Behavior Specialist

Greenfield, IN

$19 - $25.50/hr

Labcorp is seeking a Senior Primate Behaviorist to join our team in Greenfield, IN. Job ... Develop behavior management projects for study related procedures, collaborate with study directors ...

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Study Director Primate information

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$45K

$128.4K

$232.5K

How much do study director primate jobs pay per year?

As of Sep 9, 2026, the average yearly pay for study director primate 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.

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

Infographic showing various Study Director Primate job openings in the United States as of June 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $128,367 per year, or $61.7 per hour.

Study Director II

Corpus Christi, TX • On-site

RPM ReSearch
Recruiting and Staffing Services • 11 - 50 employees
Learn more about RPM ReSearchexternal

$80K - $110K/yr

Full-time

Re-posted 13 days ago

Key responsibilities

  • Oversee all phases of assigned NHP studies, including protocol development, resource planning, and scheduling.

  • Serve as the primary point of contact for study sponsors, maintaining communication throughout the project lifecycle.

  • Draft, review, and obtain approvals for study protocols, ensuring compliance with relevant regulations and SOPs.

Job description

Study Director – Non-Human Primate Research Program

Location: Corpus Christi, Texas


Job Type: Full-Time


About the Opportunity

Are you an experienced Study Director with a passion for in-vivo research and NHP (non-human primate) studies? Join our expanding research program as we build upon our existing infrastructure and create new capabilities within a collaborative, multi-site organization.

Our facility is entering an exciting phase of growth, adding innovative programs and resources to support cutting-edge biomedical research. As part of a national network of research sites, you'll have access to a broad community of experts, opportunities for cross-site collaboration, and continuous professional growth.


Key Responsibilities


Study Planning & Execution:

  • Oversee all phases of assigned studies, including protocol development, resource planning (animals and personnel), and scheduling to ensure alignment with SOPs and sponsor expectations.

Sponsor Communication:

  • Serve as the primary point of contact for study sponsors, maintaining regular, proactive communication throughout the project lifecycle.

Protocol & Compliance Oversight:

  • Draft, review, and obtain approvals for study protocols. Ensure compliance with internal SOPs, USDA regulations, the Animal Welfare Act, IACUC requirements, and the Guide for the Care and Use of Laboratory Animals.

Data & Quality Management:

  • Review and approve data collection forms, formulation instructions, and labels. Verify that all experimental data is recorded accurately and promptly address deviations or unexpected events.

Reporting & Documentation:

  • Compile and submit study results in collaboration with senior staff and principal investigators. Ensure data and specimen archiving or transfer aligns with organizational standards and sponsor requirements.

Training & Supervision:

  • Identify special methods and ensure technical staff receive appropriate training. Provide mentorship and guidance as needed.

Operational Support:

  • Be available for extended hours, holidays, and weekends as required. Support facility-wide safety and PPE compliance efforts.


Qualifications


  • Bachelor’s degree in a scientific discipline (e.g., Biology, Pharmacology, or related field).
  • 3–5 years of experience in in-vivo study execution or direction, preferably in pharmacology, pharmacokinetics, or toxicology.
  • Experience managing NHP studies is highly preferred.
  • Strong communication and organizational skills with an emphasis on sponsor-facing roles.
  • Familiarity with GLP/GCP environments is an asset, however, at this time the facility is not conducting GLP studies
  • Comfortable using digital data systems and troubleshooting common issues.


Why Join Us?


  • Innovative Environment: Be part of a growing research program focused on NHP studies.
  • Collaborative Culture: Network with professionals across multiple U.S. research sites.
  • Career Development: Access leadership support and training opportunities as the program scales.
  • Meaningful Work: Contribute to impactful biomedical research that advances health and science.


Ready to take the next step in your research leadership career?

Let's talk and help shape the future of translational research.