The Dell Medical School is looking to hire a Clinical Research Coordinator to manage and coordinate clinical research projects, ensuring compliance with regulations and facilitating the smooth execution of studies within the Texas Center for Pediatric and Congenital Heart Disease.
Requirements
- 2+ years of experience in clinical research.
- 3+ years of experience in clinical research coordination.
- Certification as a Clinical Research Coordinator (CCRC) or equivalent.
- Additional certifications in clinical research or related fields.
- Manages electronic data capture systems.
- Prepares and submits regulatory documents to IRBs and other regulatory bodies.
- Ensures adherence to Good Clinical Practice (GCP) guidelines.
Responsibilities
- Manages the day-to-day activities of clinical trials.
- Ensures compliance with study protocols and regulatory requirements.
- Coordinates participant recruitment, screening, and enrollment.
- Maintains accurate and timely documentation of study activities.
- Collects, enters, and verifies clinical trial data.
- Ensures data integrity and accuracy.
- Prepares data reports for review by the PI and sponsors.
Other
- Bachelor's Degree in health-related field.
- Master's Degree in Clinical Research, Public Health, or a related field.
- Resume/CV
- 3 work references with their contact information; at least one reference should be from a supervisor
- Letter of interest
