Clinical Research Coordinator
Core
Oversee clinical site activities, ensure patient safety and data integrity, and conduct clinical studies according to FDA/GCP and ICH regulations.
Role type
Clinical Research Coordinator II
Builds
Clinical studies and patient data
Domain
Clinical research / Life sciences
Required skills
Clinical study execution, Patient safety monitoring, Regulatory compliance (FDA/GCP/ICH), Informed consent, Vital signs measurement, Data recording, IRB coordination, Patient scheduling, Source document management
Preferred skills
BLS certification, English fluency
Technologies
EDC systems, Case report forms
Responsibilities
Conduct clinical studies per protocol, Provide medical care to patients, Schedule subject visits, Perform study activities (vital signs, ECGs, etc.), Record patient information, Obtain and maintain IRB approval, Log IP accountability, Report non-compliance, Maintain source documents
Seniority
Mid-level, hands-on IC