About this role
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 Visits. Prepares and i…
Frequently asked questions
What does a Clinical Research Associate II at Fortrea do?
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 fo…
How much does a Clinical Research Associate II at Fortrea pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Clinical Research Associate II role remote, hybrid, or on-site?
The listing is based in Singapore. Check the posting for remote or hybrid options.
How do I apply for this Clinical Research Associate II role?
You can apply directly on Fortrea's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.