Clinical Research Coordinator II
Schedule
Monday-Friday
Position Summary
The Clinical Research Coordinator II coordinates and administers clinical trials across all phases of study protocols for the Transplant and Cellular Therapy and Leukemia and Lymphoma programs. Serves as a resource for principal investigators and research team members, supporting study start-up, participant recruitment and enrollment, data collection, study-related scheduling, and subject follow-up. Oversees a diverse portfolio of clinical research studies, including CAR-T cell therapy, gene therapy, therapeutic intervention trials, observational studies, and patient registries. Assists with quality assurance and quality control activities to ensure data integrity, protocol compliance, and adherence to regulatory requirements. Provides cross-coverage and operational support for other Clinical Research Coordinators within the department.
Required Qualifications
- 3+ years experience in clinical trial coordination
- 1+ years pediatric clinical trials experience
- Bachelor's degree or associate's degree in related scientific field
- ACRP Certified Clinical Research Coordinator (CCRC) or SOCRA Certified Clinical Research Professional (CCRP) - candidates with a medical degree are exempt from certification requirement
Preferred Qualifications
- Clinical trial coordination and management experience
- Study start-up experience, including site activation and study implementation
- Regulatory experience, including IRB submissions, compliance, and study documentation
- Experience managing study budgets, contracts, and invoicing