About this role

Supports the implementation and conduct of approved research protocols
Performs study-specific research activities and/or interventions
Assists with participant recruitment, screening, informed consent/assent
Coordinates the collection and documentation of research data
Maintains regulatory documentation and study records
Supports communication between investigators, sponsors, monitors, and institutional departments
Assists investigators with the development and submission of research protocols
Contributes to study progress reports, monitoring visits, and audits

Bachelor’s degree in Clinical Research, Life Sciences, Public Health, or another healthcare-related field
Working knowledge of regulations and guidance related to clinical research (e.g., GCP, FDA regulations, IRB requirements)
Experience coordinating intergroup or multi-site clinical studies
CCRP or CCRC certification
1 or more years of relevant research experience (e.g., study coordination, site management, regulatory submissions, or clinical data management)

Clinical Research Coordinator II

Key skills