Role OverviewWorks under the direction of an Investigator(s) with limited supervision, to coordinate research projects. Coordinates regulatory documentation, schedules procedures, and maintains data collection information required for each study.
What You Will Do
Directly interacts with clinical research participants, coordinates regulatory documentation, screens, recruits, enrolls, and follows subjects according to research protocol guidelines, and maintains data collection information required for each study.
Why It Might Be a Fit
The Department of Internal Medicine is seeking a Clinical Research Coordinator II to join the Clinical Trials Unit (CTU), where you will work with clinical trials from various divisions within Internal Medicine and manage key aspects of the unit's investigational drug and device clinical trials.
Requirements
- Bachelor's Degree in medical or science related field
- 2 years years clinical research experience
- BLS (Basic Life Support) certification may be required based on research study protocols or affiliate location requirements
- CPRAED (CPR AED) certification may be required based on research study protocols or affiliate location requirements
- ACRP or SOCRA certification a plus
- Prior experience coordinating investigational drug or device clinical trials and/or industry sponsored clinical trials
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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