Clinical Research Associate
Core
Coordinate clinical trial monitoring activities, manage study documentation, and ensure compliance with regulatory requirements to support the development of treatments.
Role type
Clinical Research Associate (monitoring)
Builds
Clinical trial operations for pharmaceutical sponsors
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Clinical trial monitoring, ICH-GCP guidelines, medical data review, study documentation management, stakeholder relationship management, regulatory compliance
Preferred skills
None stated
Technologies
None stated
Responsibilities
Coordinate study setup and monitoring activities, complete study status reports, manage sponsor queries and study costs, prepare feasibility studies, ensure patient safety and regulatory compliance
Seniority
Entry-level to Mid-level (12+ months post-certification)
