Senior Clinical Research Associate

TRIO is looking for a Senior Clinical Research Associate to join their Monitoring Resources team. The role involves conducting site visits, confirming adherence to regulations, and mentoring junior team members.

Requirements

• A minimum of 2 years of monitoring experience in oncology trials
• Minimum 5 years of previous CRA experience
• Experience in monitoring early-phase trials
• Read, write and speak fluent English
• Completion of a science-related Bachelor's degree
• Excellent knowledge of medical terminology and clinical monitoring process
• Strong ICH-GCPs knowledge
• Experience with clinical trial information systems
• Ability to travel up to 60% on average
• Ability to mentor and train new/junior CRAs on-site in a positive and effective manner

Benefits

• Competitive salary
• Paid annual leave
• Health insurance plan
• Flexible working hours
• Luggage allowance
• Mobile phone allowance