Role OverviewWorks under the direction of an Investigator(s) with general supervision, to coordinate research projects. Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies.
What You Will Do
Coordinate regulatory aspects of the trial, screen, recruit, enroll and follow subjects according to protocol guidelines, maintain and coordinate data collection information required for each study.
Why It Might Be a Fit
Requires familiarity with research budgets, proficiency in clinical trial management system, electronic medical record and other required data entry systems, and 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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