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Study Director II

Study Director II

RPM ReSearchCorpus Christi, TX, US
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Job Description

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.

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    Study Director • Corpus Christi, TX, US

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