Advance cancer research from the comfort of home as a Clinical Research Associate with TRIO in Western Canada. Engage in monitoring and conducting site visits to support groundbreaking trials.
TRIO, a global leader in translational cancer research, seeks a Clinical Research Associate for its remote monitoring team. This role requires a minimum of 2 years CRA experience and includes overseeing compliance with FDA and ICH-GCP regulations. You will perform essential tasks in ensuring data integrity and mentor junior team members as needed.
Key Responsibilities: • Conduct site visits for various trial stages • Confirm adherence to regulations and guidelines • Complete and collect all necessary regulatory documents • Verify data against source documents accurately • Assist in budget negotiations and data validation
Requirements: • Bachelor’s degree in a health-related field • 2+ years of CRA experience, preferably in phase 1 trials • Robust knowledge of ICH-GCP and medical terminology • Proficient in clinical trial information systems • Ability to travel up to 60%
Use your clinical expertise to help TRIO deliver innovative cancer treatments globally. #J-18808-Ljbffr
📌 Remote Clinical Research Associate at TRIO (Winnipeg)
🏢 GL
📍 Winnipeg
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