Role OverviewWorks under the direction of an Investigator(s) with limited supervision, to coordinate research projects. Coordinates all aspects of study conduct, identifies and consents study participants, collects and manages study data, and ensures compliance with study protocols and institutional requirements.
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 and coordinates data collection information.
Why It Might Be a Fit
Requires 2 years of clinical research experience, a Bachelor's Degree in a medical or science-related field, and ACRP or SOCRA certification. May consider additional years of experience or an advanced degree in lieu of education or experience, respectively.
Requirements
- Bachelor's Degree in a medical or science-related field
- 2 years of clinical research experience
- ACRP or SOCRA certification
- BLS (Basic Life Support) certification
- CPRAED (CPR AED) certification
Benefits
- PPO medical plan
- 100% coverage for preventive healthcare
- 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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