Clinical Research Associate

If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! 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 looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in Eastern Canada. Responsibilities: * Conducting site visits, including pre-study, initiation, monitoring and termination; * Confirming adherence to all FDA, ICH-GCP and local regulations; * Ensuring the completion and collection of regulatory documents; * Performing data verification of source documents; * Ensuring implementation and compliance with FDA, 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. Qualifications: * A minimum of 2 years of monitoring experience in oncology trials * Fluent in English and French * Experience monitoring phase 1 trials * An advanced level of oncology knowledge * 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 * Fluent in both English and French What TRIO Can Offer You: * Competitive salary * 3 weeks of vacation plus paid Christmas Closure * 2 weeks paid personal/sick time * Health, Dental, Vision & Life Insurance premiums paid by TRIO * Flexible working hours * Monthly internet allowance * Up to 5% RRSP Matching Program Pay Range $105,000.00 to $140,000.00 annually - Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data. [https://assets.jazz.co/customers/customer_20191115220729_58PHFUIXCSJP484O/layout/20260313151836-image.png] [https://assets.jazz.co/customers/customer_20191115220729_58PHFUIXCSJP484O/layout/20260313151829-image.png] [https://reviews.canadastop100.com/top-employer-translational-research-in-oncology] Prior to applying please review TRIO's Applicant Information Notice [\"https://drive.google.com/file/d/1FSG55-P4-cRjLDryUzeq_Bi4800s6VqN/view?usp=drive_link\"] To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI. To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience. Teamwork · Passion · Integrity · Innovation

The Clinical Research Associate is responsible for conducting site visits, including pre-study, initiation, monitoring, and termination. They must ensure compliance with FDA and ICH-GCP regulations while managing regulatory documentation and data verification.

Candidates must have a minimum of 2 years of monitoring experience in oncology trials and a science-related Bachelor’s degree. Proficiency in both English and French is required, along with the ability to travel up to 60% of the time.

• Competitive salary • 3 weeks of vacation • Paid Christmas closure • 2 weeks paid personal/sick time • Health insurance • Dental insurance • Vision insurance • Life insurance • Flexible working hours • Monthly internet allowance • RRSP matching program

• FrenchPreferred
• Data ValidationPreferred
• EnglishPreferred

Identified from the job description. Confirm important requirements above.

• Oncology research
• Clinical monitoring
• FDA regulations
• ICH-GCP guidelines
• Regulatory documentation
• Data verification
• Budget negotiation
• Data validation
• Query resolution
• Mentoring
• Medical terminology
• Clinical trial information systems
• Phase 1 trials
• English
• French
• Regulatory Documents
• Bilingual (French/English)
• Research
• Artificial Intelligence
• Cancer Treatments
• Clinical Monitoring
• Clinical Research
• Clinical Trials
• Information Systems
• Data Validation
• Data Verification
• Equities
• Good Clinical Practices (GCP)
• Innovation
• Market Data
• Oncology
• Medical Terminology
• Mentorship
• Negotiation
• Translational Research
• Collections
• Teamwork

• Science & Research
• Healthcare
• Clinical Research Associate
• Biologists, Botanists, Zoologists and Related Professionals
• Clinical Research Coordinators
• Natural Sciences Managers

Minimum education

Bachelor’s degree

Minimum experience

2+ years

Apply by

Nov 24, 2026

Posting language

English

Working hours

40 hours per week

Location requirements

Country, CA