Clinical Research Associate (All level)

BeOne is seeking a Clinical Research Associate to execute clinical trial protocols at clinical trial sites and monitor clinical trials. The CRA will be responsible for conducting monitoring activities, identifying investigators and sites, and preparing and submitting submissions to Institutional Review Board (IRB) to obtain clinical trial authorizations and approvals.

Requirements

• BS in a relevant scientific discipline
• at least 3 years or more (CRA) monitoring experience in the pharmaceutical or CRO industry
• Excellent communication and interpersonal skills
• Excellent organizational skills and ability to prioritize and multi-task
• Fluent in English (writing and speaking)

Benefits

• Market competitive compensation package
• Performance-based annual bonus scheme
• Company shares (generous welcome grant and performance-based annual equity plan!)
• In-house and external learning and development opportunities
• Fantastic benefits program