Clinical Research Coordinator- Clinical Research and Sponsored Programs
Core
Recruits and screens patients for clinical trial eligibility, obtains informed consent, collects clinical data, and ensures regulatory compliance for multi-disciplinary research studies.
Role type
Mid-level Clinical Research Coordinator (IC)
Builds
Clinical trial data sets and regulatory documentation for sponsored research programs
Domain
Healthcare / Clinical Research
Deliverable
client delivery | dashboards & analysis
Required skills
Medical terminology, clinical research protocols, data entry accuracy, patient education, regulatory documentation, project management, database management (Excel/Access), dosage calculations
Preferred skills
CCRP certification, Epic Research Module proficiency
Technologies
Epic Research Module, Microsoft Word, Excel, Access
Responsibilities
Recruits and screens patients for protocol eligibility; Obtains informed consent and educates patients on study design; Collects and analyzes clinical test results and patient chart data; Prepares study applications and informed consent documents for ethics board approval; Coordinates billing compliance and drug accountability; Serves as liaison between patients, physicians, and regulatory bodies.
Seniority
Mid-level, hands-on IC
