Role OverviewWorks under the direction of an Investigator(s) with general supervision, to coordinate research projects. Coordinates patient/participant coordination, data management, and clinical or basic research data in support of multiple and/or complex research studies.
What You Will Do
Directly interacts with clinical research participants, coordinates regulatory aspects of the trial, schedules study procedures, screens and recruits subjects, and maintains and coordinates data collection information.
Why It Might Be a Fit
Requires knowledge of basic and clinical research terminology, regulations, and procedures, and the ability to communicate effectively with various levels of internal and external contacts.
Requirements
- Bachelor's Degree or higher degree in medical or science related field
- 1 year of clinical research experience
- BLS) BASIC LIFE SUPPORT Licensure may be required based on research study protocols or affiliate location requirements
- (CPRAED) CPR AED Licensure 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
- 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
]]>