Role OverviewWorks under the direction of an Investigator(s) to coordinate research projects, primarily performing patient/participant coordination and collecting clinical or basic research data.
What You Will Do
Coordinates regulatory aspects of trials, schedules study procedures, screens and recruits participants, and maintains data collection information.
Why It Might Be a Fit
Requires familiarity with research budgets, proficiency in clinical trial management systems, and the ability to maintain subject level documentation.
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
Benefits
- PPO medical plan
- 100% coverage for preventive healthcare
- 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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