Clinical Research Associate II - Immunology - FSP Team Madrid

Summary of

Responsibilities

Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor

requirements

, including verification of study training records.

Conducts site monitoring

responsibilities

for clinical trials according to Fortrea’s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visi…