Clinical Research Associate
Core
Conducting clinical monitoring visits, training site staff, and managing study execution for complex clinical trials.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data and site compliance for medical science studies
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical monitoring, CRF review, source document verification, query resolution, site management, feasibility research, regulatory document procurement, automated tracking system maintenance
Preferred skills
Training and mentoring, investigator meeting presentations, audit resolution, site identification
Technologies
MS Office, automated tracking systems
Responsibilities
Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits; Delivering training of investigators, site staff and project teams; Perform CRF review, source document verification and query resolution; Be responsible for site communication and management; Be involved in site identification process; Contact for clinical investigators, vendors and support services in regard to study progress; Participate in feasibility research; Preparation and delivering of presentations at Investigator's Meetings; Preparation for and attendance at company's audits; Support to Regulatory Affairs in procurement of site regulatory documents; Maintenance of study-specific automated tracking systems