Clinical Research Associate II/Sr. Clinical Research Associate

Overview

Role involves monitoring and managing clinical studies at investigative sites.

Ideal candidate has 2+ years of CRA experience in CRO or pharmaceutical industry and oncology monitoring.

Locations

• Canada

Requirements

• 4-year degree or equivalent experience
• 2+ years CRA experience for CRA II
• 4+ years CRA experience for Sr. CRA
• Experience in monitoring oncology
• Availability for 50-60% travel
• Fluency in English

Responsibilities

• Monitor clinical studies
• Coordinate study setup
• Interact with clients
• Support Project Managers
• Identify study risks

Benefits

• Paid time off
• Volunteer time off
• Robust medical offerings
• 401k with company match
• Paid parental leave