Clinical Research Associate I or II
Core
Overseeing and coordinating clinical trials, ensuring regulatory compliance, and collecting/analyzing critical data to bring new medicines to patients.
Role type
Clinical Research Associate (monitoring & data management)
Builds
Clinical trial studies for pharmaceutical sponsors
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
ICH-GCP guidelines knowledge, medical data review, study coordination, regulatory compliance, stakeholder management, travel logistics
Preferred skills
None stated
Technologies
None stated
Responsibilities
Coordinate study setup and monitoring activities; manage sponsor queries and study cost efficiency; prepare and review study documentation and feasibility studies; ensure patient safety and regulatory compliance; maintain relationships with clinical investigators and site staff.
Seniority
Individual Contributor (I or II level)
