Clinical Research Associate

Translational Research in Oncology; Edmonton; Remote; CAD 100,000 - 123,000; Full time

Benefits offered by this job

Annual raise

Vacation time 3 weeks

Personal/sick time 10 days

Volunteer day

Health insurance

RRSP matching

Flexible hours

Internet allowance

Home office allowance

Maternity top-up

Employee assistance

Referral bonus

Job summary

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join the Monitoring Resources team. This remote position covers Western Canada, including BC, Alberta, Saskatchewan or Manitoba, and reports to the CRA Line Manager.

You will conduct site visits, verify data, ensure ICH-GCP compliance, assist with budgets, and mentor junior staff. Qualifications include a Bachelor's in allied health, 2+ years CRA experience, Phase 1 trial monitoring, and strong English; French

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; French is preferred but not required

Responsibilities

• Conducting site visits, including pre-study, initiation, monitoring and termination
• Confirming adherence to 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

Skills

CRA experience

English fluency

Medical terminology

ICH-GCP knowledge

Travel readiness

Teamwork

French (optional)

Education

Bachelor's degree in allied health

Tools

Clinical trial systems

Job description

Translational Research in Oncology (TRIO)is a global clinical research organizationdedicated 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 2years 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 InternetAllowance to support working from home
• One-time Home Office Allowance
• MaternityLeave 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