Role OverviewWorks under the direction of an Investigator(s) to provide ongoing data management for local and national research studies. May coordinate observational (non-treatment/treatment) trials/studies. Provides supporting role for more complex studies under the direction of the PI, Clinical Research Coordinator and/or Clinical Research Lead.
What You Will Do
Assists research staff by completing research protocol related tasks, reviews and abstracts information from medical records, enters data into case report forms, and assists with data queries and possible edits for accuracy.
Why It Might Be a Fit
Requires 2 years experience with High School Diploma or 1 year experience with Associate's Degree. Must have High School Diploma or Associate's Degree in medical or science related field or Bachelor's Degree in medical or science related field and no prior experience.
Requirements
- High School Diploma or Associate's Degree in medical or science related field
- 2 years experience with High School Diploma or 1 year experience with Associate's Degree
- (BLS) BASIC LIFE SUPPORT may be required based on affiliate location requirements.
- (CPRAED) CPR AED may be required based on affiliate location requirements.
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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