Senior Business Analyst - Information and Data Management to implement records lifecycle management

s i systems; Edmonton; Remote; CAD 100,000 - 123,000; Full time

Benefits offered by this job

Annual compensation review

3 weeks vacation plus December closure

10 days paid personal/sick time

1 paid volunteer day per year

Health, Dental, Vision & Life premiums

Job summary

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join our Monitoring Resources team. The role is remote based in Western Canada, with travel as needed, reporting to the CRA Line Manager.

The candidate will conduct site visits, ensure regulatory compliance, and support data verification and mentoring within a dynamic clinical research environment. Minimum 2 years CRA experience is required, with a Bachelor's in allied health fields.

Qualifications

• Bachelor's degree in allied health fields or international equivalent.
• Minimum 2 years of CRA experience.
• Fluent in English; French is preferred but not required.

Responsibilities

• Conduct site visits including pre-study, initiation, monitoring, and termination.
• Ensure adherence to FDA, ICH-GCP, and local regulations.
• Verify data against source documents and resolve queries.
• Mentor junior team members as required.
• Support budget negotiations and follow-up where applicable.

Skills

Medical terminology

Clinical monitoring process

ICH-GCP knowledge

Education

Bachelor's degree in allied health fields

Tools

Clinical trial information systems

Job description

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.

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