Clinical Research Associate
Core
Managing and monitoring national and international clinical studies to ensure compliance with Good Clinical Practice (GCP), study protocols, and applicable regulations.
Role type
Certified Clinical Research Associate (CRA)
Builds
Clinical trials for pharmaceutical, biotech, and medical device sectors
Domain
Clinical research and regulatory compliance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GCP knowledge, regulatory compliance, data accuracy verification, site monitoring, deviation management, audit support
Preferred skills
Project management collaboration, risk assessment, report preparation
Technologies
Clinical trial management systems, regulatory databases
Responsibilities
Conduct site monitoring activities (SIV, SQV, IMV, COV), verify protocol adherence, ensure data accuracy, support site operational management, monitor study progress and prepare documentation, manage deviations and risks, support regulatory audits
Seniority
Mid-level, hands-on IC
