Clinical Research Associate

4 days ago

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501 - 1000

Description

• Executes clinical monitoring activities at clinical trial sites • Monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs • Performs monitoring activities related to selection, initiation, conduct, and timely completion of oncology/hematology clinical trials • Collaborates closely with the Regional Clinical Operations Manager to ensure study timelines and quality standards are maintained • Conducts monitoring visits per monitoring plan and SOPs • Completes monitoring visit reports according to ICH-GCP and BeiGene standards • Manages site performance and ensures inspection readiness of the study

Requirements

• BS in a relevant scientific discipline • Minimum of 2 years of monitoring experience • Experience in oncology and Hematology global trials preferred