Role OverviewWorks under the direction of an Investigator(s) to coordinate research projects, primarily performing patient/participant coordination and data management.
What You Will Do
Collects and ensures quality control of clinical or basic research data, interacts with clinical research participants, and coordinates regulatory aspects of trials.
Why It Might Be a Fit
This role requires 1 year of clinical research experience and a Bachelor's Degree or higher in a medical or science-related field. ACRP or SOCRA certification is a plus.
Requirements
- Bachelor's Degree or higher in medical or science-related field
- 1 year of clinical research experience
- BLS (Basic Life Support) Licensure may be required
- CPRAED (CPR AED) Licensure may be required
- ACRP or SOCRA certification a plus
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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