Market Research Participant

gl; Edmonton; Teletrabalho; CAD 100 000 - 123 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Annual raise

3 weeks vacation

Paid personal/sick time

Volunteer day

Benefits package

RRSP matching

Flexible hours

Internet allowance

Home office allowance

Maternity top-up

Family assistance

Referral bonus

Resumo da oferta

Translational Research in Oncology (TRIO) seeks a Clinical Research Associate to join our Monitoring Resources team. This remote role supports Western Canada, travel up to 60% as needed to monitor sites and ensure regulatory compliance.

Reporting to the CRA Line Manager, you will conduct site visits, verify data, manage regulatory documents, and collaborate across teams to advance clinical trials while ensuring ICH-GCP adherence.

Qualificações

• 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

Responsabilidades

• 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

Conhecimentos

Clinical trial monitoring

ICH-GCP knowledge

Medical terminology

CTMS experience

English fluency

French language (preferred)

Travel willingness

Formação académica

Bachelor's degree in allied health fields

Descrição da oferta de emprego

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.

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.

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 per 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

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 To support efficiency, TRIO may use limited AI tools during the candidate review process.