CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs
Job Summary
CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs.
CRA is responsible for collaborating closely with the Country and Regional Clinical Study Teams to ensure study timelines are adhered to and required quality standards are maintained.
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals.
Matching Summary
CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs.
Skills & Requirements
Must-have
ICH guidelines and GCP
Oncology/onco-hematology clinical trials
Site selection and evaluation
Monitoring visits and reporting
Trial Master File (TMF) maintenance
Inspection readiness
Nice-to-have
Scientific and business professionals
Highly motivated, collaborative
Passionate interest in fighting cancer
Operating excellence and innovation
Mentoring junior staff
Key Requirements
3-5 years of monitoring experience
BS in scientific or healthcare discipline preferred
Oncology/onco-hematology global trials experience preferred