Clinical Research Study Coordinator Services
The CTRC employs research study coordinators across all clinical disciplines. Our staff can assist investigators with Institutional Review Board (IRB) submissions and follow-up; participant screening and enrollment; all study procedures and documentation; adverse event reporting; blood draws, infusions, and ECGs; continuing reviews and modifications to approved research and study closure.
The CTRC offers comprehensive study coordination services for studies across all clinical disciplines, including:
- IRB submissions, including pre-review of regulatory documents and follow-up (Clinical Investigator Resource Core)
- Participant screening and enrollment
- All study procedures and documentation
- Adverse event reporting
- Blood draws, infusions, and ECGs
- Continuing reviews and modifications to approved research and study closure
- Specimen packaging and shipping services
- Pharmacokinetic and pharmacodynamic studies
- Electrocardiograms
- Administration of research questionnaires
- Data acquisition
- Specimen storage