Clinical Research Associate
Core
Conduct clinical trial monitoring to ensure study compliance, patient safety, and data accuracy across clinical programmes.
Role type
Clinical Research Associate (monitoring)
Builds
Clinical trial operations and study execution
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Clinical trial monitoring, ICH-GCP guidelines, medical data review, stakeholder relationship management, regulatory compliance
Preferred skills
None stated
Technologies
None stated
Responsibilities
Coordinate study setup and monitoring activities; manage sponsor queries and study costs; prepare and review study documentation and feasibility studies; ensure compliance with procedures, protocols, and regulatory requirements.
Seniority
Individual Contributor
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