Clinical Research Coordinator I, Pediatrics

Job Summary

Works under the direction of an Investigator(s) with general supervision, to coordinate research projects. This position primarily performs patient/participant coordination, however, may conduct data management in smaller departments on as needed basis. Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies. The Clinical Research Coordinator I will be responsible for updated and maintaining CRF's, study data, consenting and enrolling patients for 7 active studies, maintaining regulatory compliance to UTSW HRPP standards, and collaborating with other institutions on study related information and best practices.

Benefits

UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include: PPO medical plan, available day one at no cost for full-time employee-only coverage100% coverage for preventive healthcare-no copayPaid Time Off, available day oneRetirement Programs through the Teacher Retirement System of Texas (TRS)Paid Parental Leave BenefitWellness programsTuition ReimbursementPublic Service Loan Forgiveness (PSLF)

Required EXPERIENCE AND EDUCATION

• Education: Bachelor's Degree or higher degree in medical or science related field
• Experience: 1 year of clinical research experience
• May consider additional years of experience or advanced degree in lieu of education or experience, respectively.

Preferred

• Licenses and Certifications: (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

Job Duties

• Directly interacts with clinical research participants, as required, for the research study. Interacts via telephone, telehealth or in-person.
• Collaborate with other institutions on study related information and best practices.
• Directly interacts with or cares for patients; directly interacts with or cares for human-subjects research participants; regularly maintains, modifies, releases or similarly affects patient records (including patient financial records); or regularly maintains, modifies, releases or similarly affects human-subjects research records.
• Performs other duties as assigned.