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 - Strong 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 creative cancer treatments globally.#J-18808-Ljbffr

📌 Remote Clinical Research Associate At Trio (Winnipeg)
🏢 GL
📍 Winnipeg