Clinical Research Associate
Core
Conduct monitoring visits and manage activities for clinical trials from Phase I to Phase IV, serving as the main communicator between sponsors and investigators.
Role type
Clinical Research Associate
Builds
Clinical trial monitoring and management activities
Domain
Biomedical research and clinical trials
Deliverable
client delivery
Required skills
Clinical trial monitoring, SOP implementation, adverse event management, ethics committee communication, trial master file maintenance, project coordination
Preferred skills
Good Clinical Practice training, Master's in Monitoring/Coordination
Technologies
Monitoring tools, trial master files
Responsibilities
Conduct initial, follow-up, and closing monitoring visits; prepare visit reports; manage adverse events and medication; communicate between sponsor and investigator; maintain trial master files; support researcher meetings and workshops
Seniority
Entry-level to Junior