Principal Clinical Trials Coordinator (SAN ANTONIO)
University HealthUSjob_description.job_card.1_day_ago
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job_description.job_card.job_descriptionRequired : 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.
Find out more about the daily tasks, overall responsibilities, and required experience for this opportunity by scrolling down now.
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 :
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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