Clinical Study Coordinator
Core
Supports a medical institution in clinical trial-related activities, including feasibility assessment, patient recruitment, data entry, and regulatory document submission.
Role type
Clinical Study Coordinator (Site/Study Coordinator)
Builds
Clinical trial operations at medical sites
Domain
Healthcare / Clinical Research
Required skills
patient recruitment, data entry, regulatory document preparation, investigational product handling, scheduling, training coordination, adverse event reporting
Preferred skills
ACRP or SOCRA certification, GCP certification, IATA certification, phlebotomy
Technologies
EDC systems
Responsibilities
Facilitate evaluation of proposed studies, assist with patient recruitment and eligibility confirmation, ensure accurate data entry into EDC systems, support handling and reconciliation of investigational products, assist with scheduling sponsor/CRO visits, prepare regulatory documents for IRBs and authorities, maintain study documents for audits.
Seniority
Mid-level, hands-on IC