Remote Clinical Research Associate at TRIO

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 innovative cancer treatments globally.