Clinical Research Associate I or II
Core
Overseeing and coordinating clinical trials, ensuring regulatory compliance, and collecting/analyzing critical data to support treatment development.
Role type
Clinical Research Associate (IC)
Builds
Clinical trial studies and associated data packages
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
ICH-GCP guidelines knowledge, medical data review and evaluation, study setup and monitoring, query resolution, study documentation management, feasibility study preparation
Preferred skills
None stated
Technologies
None stated
Responsibilities
Coordinate study setup and monitoring activities; complete accurate study status reports and maintain documentation; run sponsor-generated queries; prepare and review study documentation and feasibility studies; ensure patient safety and regulatory compliance
Seniority
Entry to Mid-level, hands-on IC