Clinical Research Associate
Core
Perform monitoring and site management to ensure clinical studies are conducted per protocol and regulations.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for life sciences sponsors
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
Site monitoring, subject recruitment tracking, protocol administration, regulatory compliance (GCP/ICH), TMF/ISF management, data query resolution, financial management
Preferred skills
Therapeutic knowledge, project start-up support
Technologies
Microsoft Word, Excel, PowerPoint, laptop, iPhone, iPad
Responsibilities
Conduct site monitoring visits (selection, initiation, monitoring, close-out), track subject recruitment and enrollment, administer protocol training to sites, evaluate site practice quality, manage study progress and documentation, liaise with study teams
Seniority
Mid-level, hands-on IC