Clinical Research Associate

Translational Research in Oncology; Remote; CAD 110,000 - 130,000; Full time

Job summary

A global clinical research organization is seeking a Clinical Research Associate to join its Monitoring Resources team. This home-based position in Ontario requires a minimum of 2 years of monitoring experience in oncology trials and completion of a science-related Bachelor's degree. Responsibilities include conducting site visits and ensuring compliance with regulatory standards. TRIO offers competitive salary, flexible hours, and various employee benefits, including health insurance and RRSP matching.

Benefits

Competitive salary

3 weeks of vacation plus paid Christmas Closure

Health, Dental, Vision & Life Insurance premium paid by TRIO

Monthly internet allowance

Home office allowance

Up to 5% RRSP Matching Program

Qualifications

• Minimum of 2 years of monitoring experience in oncology trials.
• Experience monitoring phase 1 trials.
• Strong knowledge of medical terminology and clinical monitoring process.

Responsibilities

• Conducting site visits, including pre-study, initiation, monitoring and termination.
• Confirming adherence to all FDA, ICH-GCP and local regulations.
• Mentoring junior team members as required.

Skills

Monitoring experience in oncology trials

Fluent in English

Strong ICH-GCPs knowledge

Ability to travel

Education

Bachelor's degree in a science-related field

Tools

Clinical trial information systems

Job description

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 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 Ontario.

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

• Minimum of 2 years of monitoring experience in oncology trials
• Experience monitoring phase 1 trials
• Fluent in English
• 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 French preferred, but not mandatory

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 premiumspaid by TRIO
• Flexible working hours
• Monthly internet allowance
• Home office allowance
• Luggage allowance
• Up to 5% RRSP Matching Program

Pay Range: $110,000 - $130,000 CAD - Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.

We thank all candidates for their interest; only those selected for an interview will be contacted.

Teamwork · Passion · Integrity · Innovation

Prior to applying please review TRIO's Applicant Information Notice

Teamwork · Passion · Integrity · Innovation