Role OverviewWorks under the direction of an Investigator(s) to coordinate research projects, primarily performing patient/participant coordination and collecting and ensuring quality control of clinical or basic research data.
What You Will Do
Coordinate regulatory aspects of the trial, schedule study procedures, screen and recruit participants, maintain and coordinate data collection information, and assist in developing and implementing research studies.
Why It Might Be a Fit
Requires familiarity with research budgets, data management, and electronic medical records, with a focus on patient safety and research protocol adherence.
Requirements
- Bachelor's Degree or higher degree in medical or science related field
- 1 year of clinical research experience
- BLS (Basic Life Support) Licensure
- CPRAED (CPR AED) Licensure
- ACRP or SOCRA certification a plus
Benefits
- PPO medical plan
- 100% coverage for preventive healthcare-no copay
- Paid Time Off
- Retirement Programs through the Teacher Retirement System of Texas (TRS)
- Paid Parental Leave Benefit
- Wellness programs
- Tuition Reimbursement
- Public Service Loan Forgiveness (PSLF) Qualified Employer
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