Study Director (SD I/II/III/Senior SD) at Texas Biomedical Research Institute

San Antonio, Texas, United States -

Full Time

Start Date

Immediate

Expiry Date

10 Feb, 26

Salary

0.0

Posted On

12 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Study Director, Preclinical Studies, Data Analysis, GLP Compliance, Biosafety Level 3, Biosafety Level 4, Animal Models, Pharmacokinetics, Quality Assurance, SOP Development, Team Collaboration, Talent Acquisition, Mentoring, Scientific Research, Biomedical Sciences, Immunology

Industry

Research Services

Description

Description Study Director (SD I/II/III/Senior SD) Texas Biomed is actively recruiting an experienced Study Director to join its Applied Science and Innovation (ASI) Division. We are looking for individuals with pre-clinical Study Director experience who are eager to contribute to a dynamic, fast-paced, and internationally important organization performing GLP and animal rule biocontainment research in support of developing diagnostics, therapies, and vaccines to protect our nation. The successful candidate will also help contribute to training programs and enhanced technical capacity to support Texas Biomed’s mission of advancing global health and biodefense research. Applicants with experience and a track record of success will be prioritized, especially in biosafety level 3 and 4. The Role: Serve as Study Director for preclinical studies involving small animals (rodents, ferrets), non-human primates (NHPs), and other animal models. Interpret and integrate in-life, clinical, and laboratory data to write high-quality final study reports from outline through submission. Analyze bioanalytical and pharmacokinetic (PK) data, and interface with bioanalytical teams and regulatory sponsors. Support studies across diverse therapeutic modalities, including vaccines, therapeutic monoclonal antibodies, and metabolic drugs. Collaborate with Quality Assurance and regulatory teams to maintain compliance with GLP and other regulatory standards. Contribute to the build-out of GLP study capabilities, including: Training and mentoring of junior study staff Development of SOPs and study workflows Input on assay qualification, staffing needs, and facility readiness Interface with cross-functional teams, including BSL-4 operations, to ensure safe and efficient performance of complex regulated studies. Provide insights on talent acquisition, retention, and performance management, including promotions, reviews, and salary adjustments, to support team growth and development. Our Ideal Candidate: Ph.D., D.V.M., or equivalent in biomedical sciences, microbiology, virology, immunology, or a related field. Proven experience as a Study Director. Excitement to contribute to the growth and expansion of a GLP-compliant infrastructure at Texas Biomed. A strong publication record is desirable, demonstrating contributions to scientific advancements. Hands-on experience in BSL-3 and BSL-4 environments is strongly preferred, with a deep understanding of biocontainment protocols. How to Apply? To be considered for the position you must upload two documents when applying to this job ad, in addition to completing the application: Résumé or CV A Cover Letter addressed to Gregory Ippolito Who We Are: Join our incredible mission to pave the way for a world free from the fear of infectious disease! Texas Biomedical Research Institute is pioneering and sharing scientific research to protect you, your families, and our global community from the threat of infectious diseases. Our scientific discoveries create breakthroughs in medical research to provide better overall global health. Texas Biomed is the only independent, nonprofit infectious disease research institute in the U.S. to combine: The highest-level biocontainment labs for infectious disease and biodefense research A federally-designated National Primate Research Center More than 80 years of discoveries advancing diagnostics, vaccines and therapies An entrepreneurial culture and specialized expertise in regulated science required for FDA approval What We Can Offer You: Recognized as one of the San Antonio Business Journal’s Best Places to Work in 2025. Awarded the 2024 Healthy Workplace Platinum Recognition by the San Antonio Business Group on Health (SABGH). Employee-centered culture focused on open communication, job empowerment, and trust. Comprehensive health, dental, vision, and life insurance plans for you and your family (including your pets!). Competitive employer-funded retirement plan with 7% contributions starting on day one, increasing with years of service. Generous paid time off, including 14 paid holidays and a paid Winter Recess (last week of December until New Year’s). On-site medical clinic, wellness incentives, and paid prescription drug resources to support your health. On-site gym and wellness programs to help you stay active. Flexible work arrangements designed to support work-life balance. We offer a relaxed dress code so you can feel comfortable and be yourself at work. Dynamic learning environment with professional development, mentorship, tuition reimbursement, and leadership programs to help you grow. We take pride in fostering a culture of respect, opportunity, and unity. Texas Biomedical Research Institute provides equal employment opportunities for all qualified employees and applicants without regard to race, color, sex, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.

Responsibilities

Serve as Study Director for preclinical studies involving various animal models and write high-quality final study reports. Collaborate with cross-functional teams to ensure compliance with GLP and other regulatory standards.