Clinical Research Coordinator
Core
Ensuring smooth conduct of clinical trials while maintaining participant care, data quality, and regulatory compliance.
Role type
Clinical Research Coordinator
Builds
Clinical trials
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Participant recruitment and screening, Informed consent management, Clinical procedures (vital signs, ECGs, sample collection), Data entry and management in EDC/IRT systems, Regulatory compliance (ICH-GCP), Source documentation maintenance, Study milestone tracking, Risk management, AE/SAE reporting
Preferred skills
Experience transitioning from nursing or health sciences
Technologies
EDC systems, IRT systems
Responsibilities
Coordinating day-to-day clinical trial activities per study protocols, Managing participant recruitment, screening, and follow-up, Performing clinical procedures including vital signs and sample collection, Maintaining accurate source documentation and Investigator Site Files, Liaising with investigators, sponsors, and CRAs, Responding to study queries and monitoring actions, Supporting study milestone tracking and quality improvement initiatives, Assisting with supervision of Clinical Trial Assistants, Ensuring participant safety through AE/SAE reporting
