Senior Clinical Coordinator - Advance the Future of Clinical Research (SAN ANTONIO)University Health • SAN ANTONIO, Texas, US
Senior Clinical Coordinator - Advance the Future of Clinical Research (SAN ANTONIO)
University Health • SAN ANTONIO, Texas, US
[job_card.30_days_ago]
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- [job_card.full_time]
[job_card.job_description]Bachelors of Science in Nursing (BSN) from an accredited institution Minimum 3 years of clinical research experience Working knowledge of research methods and federal regulations for human subject research Must possess or qualify to obtain CCRP or CCRA certification within 6 months of hire Strong leadership and judgment in confidential, regulatory, and ethical matters Ability to navigate complex research protocols with a sharp eye for detail Confident representing the department in multi-institutional settings Excellent communication, planning, and coordination skills A dynamic, collaborative, and mission-driven environment Opportunities to lead and influence policy at the institutional and national levels A commitment to professional development and clinical research excellence The chance to make a real impact on groundbreaking studies and healthcare transformation Bring your skills, passion, and vision to a team thats shaping the future of healthcare research. Apply today to become our Senior Clinical Research Coordinator.
Senior Clinical Research Coordinator
Location : University Health
Full-Time - Day Shift
Advance the Future of Clinical Research
Are you passionate about clinical research and ready to take your expertise to the next level? At University Health, were seeking a Senior Clinical Research Coordinator to lead and support high-impact studies that shape the future of patient care. This is a unique opportunity to bring your clinical insight and research experience to a role that supports innovation, compliance, and excellence in human subject research.
What Youll Do
As a Senior Clinical Research Coordinator , youll play a vital leadership role in the coordination and review of complex human subject research protocols. You will :
- Evaluate and provide expert clinical and risk assessment on research protocols and procedures
- Assist the Director with implementing a robust Human Subjects Protection Program
- Serve as a departmental representative to internal and external research committees, including IRB and OHRP
- Coordinate, monitor, and educate staff on best practices in research compliance and study execution
- Support grant applications, budgeting, and program planning across diverse research initiatives
What Were Looking For
Education & Experience :
Required :
Core Competencies :
Why Join Us?
At University Health, youll be part of a team that is passionate about research, innovation, and improving patient outcomes. We offer :
Ready to Elevate Clinical Research?
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