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 studiesComfortable 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.