Role OverviewWorks under the direction of an Investigator(s) with general supervision, to coordinate research projects. This position primarily performs patient/participant coordination, however, may conduct data management in smaller departments on as needed basis.
What You Will Do
Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies.
Why It Might Be a Fit
The ideal candidate will possess strong organizational and communication skills, experience with clinical research data management, familiarity with imaging-based research workflows, and basic programming or coding experience to support data quality and operational efficiencies.
Requirements
- Bachelor's Degree or higher degree in medical or science related field
- 1 year of clinical research experience
- BLS (BASIC LIFE SUPPORT) Licensure may be required based on research study protocols or affiliate location requirements.
- CPRAED (CPR AED) Licensure may be required based on research study protocols or affiliate location requirements.
- ACRP or SOCRA certification a plus
Benefits
- PPO medical plan
- 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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