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. Assists in developing and implementing research studies.
What You Will Do
Directly interacts with clinical research participants, coordinates data management, and assists in developing and implementing research studies. May conduct data management in smaller departments on an as-needed basis.
Why It Might Be a Fit
Requires at least two years of clinical research experience and a comprehensive understanding of research regulations, study operations, participant management, and data integrity. The CRC II serves as a key liaison among investigators, sponsors, participants, and institutional departments to ensure the successful conduct of clinical research.
Requirements
- Bachelor's Degree in medical or science related field
- 2 years years clinical research experience
- BLS (Basic Life Support) or CPR AED may be required based on research study protocols or affiliate location requirements
- ACRP or SOCRA certification a plus
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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