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
• Solid 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.
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📌 Remote Clinical Research Associate at TRIO (Alberta)
🏢 GL
📍 Alberta
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