Role OverviewWorks under the direction of an Investigator(s) with general supervision, to provide ongoing data management for local and national research studies and may coordinate observational (non-treatment/treatment) trials/studies. May provide supporting role for more complex studies under the direction of the PI, Clinical Research Coordinator and/or Clinical Research Lead.
What You Will Do
Primary duties will include patient recruitment, consenting, data collection, data entry, biospecimen collection and processing, query resolution, and overall regulatory management.
Why It Might Be a Fit
This position will be part of a collaborative team environment.
Requirements
- High School Diploma or Associate's Degree in medical or science related field
- Bachelor's Degree medical or science related field and no prior experience
- 2 years experience with High School Diploma or 1 year experience with Associate's Degree
- Licenses and Certifications: (BLS) BASIC LIFE SUPPORT may be required based on affiliate location requirements.
- (CPRAED) CPR AED may be required based on affiliate location requirements.
Benefits
- PPO medical plan, available day one at no cost for full-time employee-only coverage
- 100% coverage for preventive healthcare-no copay
- Paid Time Off, available day one
- 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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