Clinical Research Associate-Freelance

Translational Research in Oncology • Montreal, QC

11d • Remote

About The Position

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is seeking a Clinical Research Associate (CRA) to join our Monitoring Resource team. This is a remote, part-time freelance opportunity on a 6-month contract, open to candidates based in Canada.

Requirements

• A minimum of 2 years of monitoring experience in oncology trials
• Fluent in French and English
• Completion of a science-related Bachelor’s degree
• Excellent knowledge of medical terminology and clinical monitoring process
• Strong ICH-GCPs knowledge
• Experience with clinical trial information systems
• Ability to travel up to 60% on average
• Must be legally authorized to work in the country

Nice To Haves

• Experience monitoring in early-phase trials will be valued.

Responsibilities

• Performing data verification of source documents
• Conducting site visits, including pre-study, initiation, monitoring, and termination
• Confirming adherence to all FDA, ICH-GCP, and local regulations
• Ensuring implementation and compliance with FDA, and ICH-GCP guidelines
• Participating in budget negotiation and follow-up where applicable
• Assisting with data validation and query resolution
• Mentoring junior team members as required
• Ensuring the completion and collection of regulatory documents

What This Job Offers

• Job Type: Part-time
• Career Level: Mid Level