TRIO - Translational Research in Oncology

Clinical Research Associate

Alberta, Canada, British Columbia, Canada, Manitoba, Canada, Saskatchewan, Canada
Remote
Posted Oct 8, 2026
1 position

$100,000–$122,500 / year

Opens an external site

Employment type: Full-time
Experience level: Mid-level · 2+ years
Minimum education: Bachelor’s degree
Apply by: Jan 4, 2027
Posting language: English
Working hours: 40 hours per week

Job summary

The Clinical Research Associate is responsible for conducting site visits, ensuring compliance with FDA and ICH-GCP regulations, and performing data verification. They will also assist with budget negotiations, data validation, and mentoring junior team members.

Job details

Translational Research in Oncology (TRIO) is a global 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 the CRA Line Manager, this position will be remote based in Western Canada (British Columbia, Alberta, Saskatchewan, or Manitoba). This is an upcoming vacancy, and we are currently accepting applications. 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: Bachelor's Degree in allied health fields such as Medical, Nursing, Pharmacy, or Health Science – or its international equivalent Minimum 2 years of previous CRA experience Experience monitoring phase 1 trials 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 work both independently and in a team environment Read, write and speak fluent English required Fluent in French is preferred, but not required What TRIO Can Offer You: Annual compensation review with opportunities for professional growth 3 weeks of vacation plus paid December Holiday Closure 10 days paid personal/sick time 1 paid volunteer day / year A rich benefit plan with Health, Dental, Vision & Life Insurance premiums paid by TRIO Up to 5% RRSP Matching Program Flexible working hours to promote work-life balance Monthly Internet Allowance to support working from home One-time Home Office Allowance Maternity Leave Top-Up Program Employee Family Assistance Program to support you and your family during difficult times Employee Referral Bonus Program Pay Range: $100,000.00 to $122,500.00 - Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data. Teamwork · Passion · Integrity · Innovation Prior to applying please review TRIO's Applicant Information Notice 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

What you’ll do

Requirements

Candidates must hold a Bachelor's degree in an allied health field and possess a minimum of 2 years of CRA experience. Proficiency in medical terminology, clinical monitoring processes, and experience with Phase 1 trials are required.