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. Maintains databases, completes data abstraction and queries, and prepares for study visits.
Why It Might Be a Fit
This position will be responsible for screening patients for study eligibility, supporting the CF plus team in building redcap projects, and ensuring studies remain compliant with all regulatory requirements.
Requirements
- Bachelor's Degree or higher degree in medical or science related field
- 1 year of clinical research experience
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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