Clinical Research Monitor
Core
Monitor clinical research at investigational sites to ensure compliance with study protocols, regulatory requirements, and ethics committee policies.
Role type
Clinical Research Monitor (Medical Device)
Builds
Clinical studies for medical device innovation
Domain
Healthcare / Medical Devices
Deliverable
client delivery
Required skills
Clinical trial monitoring, regulatory compliance (GCP), relationship management with investigators/CROs, adverse event review, study documentation, investigator training, patient recruitment support
Preferred skills
Medical device industry experience, problem-solving, multi-project management
Technologies
Microsoft Office, IT tools for clinical research
Responsibilities
Monitor clinical trial progress and documentation; Develop relationships with clinical investigators and research institutions; Review adverse events and monitor study timelines/budgets; Prepare study documentation and status reports; Train investigators and site personnel; Support clinical development strategy and patient recruitment
Seniority
Mid-level, hands-on IC