Role OverviewWorks under minimal supervision to manage and conduct regulatory monitoring reviews of Research Administration functions. Performs complex monitoring, assurance, and administrative activities for IRB-approved human research studies.
What You Will Do
Conducts complex assurance/effectiveness reviews of compliance activities, reviews ClinicalTrials.gov submissions, and provides guidance to Sponsor Investigator for their regulatory activities.
Why It Might Be a Fit
Requires 3 years of professional experience in research compliance, knowledge of federal regulations governing research, and a Bachelor's Degree in a related area.
Requirements
- Bachelor's Degree degree in science, nursing, public health, biology, pharmacy, healthcare administration, or related area
- 3 years of professional experience in research compliance
- Knowledge of federal regulations governing research
- Certification/coursework completion in clinical research monitoring or healthcare compliance is preferred
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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