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Clinical Research Associate Intern Jobs in Quebec

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Senior Clinical Research Associate

Montreal, QC · On-site +1

As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported ...

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Clinical research associate II

Montreal, QC · On-site

Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. * Strong organizational and communication ...

AbCellera

Clinical Study Start Up Manager

Montreal, QC · On-site

Collaborating closely with Clinical Research Associates (CRAs), Clinical Project Managers (CPMs), and other internal stakeholders to provide start-up updates, mitigate risk, and transition sites ...

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All JobsClinical Research Associate Intern JobsClinical Research Associate Intern Jobs in Quebec

Clinical Research Associate Intern information

See Quebec salary details

$8

$31

$64

How much do clinical research associate intern jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical research associate intern in Quebec is $31.55, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $40.62 per hour, depending on experience, location, and employer.

What does a clinical research associate intern do?

A Clinical Research Associate Intern assists in the monitoring and coordination of clinical trials to ensure they are conducted according to regulatory standards and study protocols. Interns may help with site visits, data collection, documentation, and communication between research teams and sponsors. This role provides hands-on experience in clinical research processes and helps interns develop an understanding of Good Clinical Practice (GCP) guidelines. Interns often work under the supervision of experienced clinical research professionals and gain valuable insight into the pharmaceutical or medical device industry.

What are the key skills and qualifications needed to thrive as a clinical research associate intern, and why are they important?

To thrive as a Clinical Research Associate Intern, you need a solid understanding of clinical trial protocols, regulatory guidelines (like GCP), and typically a background in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certifications like GCP training are highly valued. Strong attention to detail, organizational skills, and effective communication help interns excel in monitoring studies and collaborating with site staff. These skills are crucial for ensuring data integrity, regulatory compliance, and the smooth operation of clinical research projects.

What typical challenges do clinical research associate interns encounter when monitoring clinical trial sites?

Clinical Research Associate Interns often face challenges such as ensuring accurate data collection, maintaining regulatory compliance, and communicating effectively with site staff. Balancing these responsibilities while learning industry protocols can be demanding, especially when managing multiple sites or studies. Interns are supported by experienced team members, but must quickly adapt to varying site workflows and documentation standards to ensure trial integrity.

What is the difference between Clinical Research Associate Intern vs Clinical Research Coordinator?

AspectClinical Research Associate InternClinical Research Coordinator
Required CredentialsTypically pursuing or holding a degree in life sciences; some internships require minimal certificationsUsually holds a bachelor's degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentInternship setting within pharmaceutical companies or research institutions; supervised learningActive role in clinical trial sites; responsible for daily trial operations
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for trainingEmployed directly at clinical sites, hospitals, or research centers

While both roles involve clinical trial processes, a Clinical Research Associate Intern is primarily a learning position focusing on gaining experience, whereas a Clinical Research Coordinator manages the day-to-day operations of clinical trials at research sites.

What are popular job titles related to Clinical Research Associate Intern jobs in Quebec?

For Clinical Research Associate Intern jobs in Quebec, the most frequently searched job titles are:

What job categories do people searching Clinical Research Associate Intern jobs in Quebec look for?

The top searched job categories for Clinical Research Associate Intern jobs in Quebec are:

What cities in Quebec are hiring for Clinical Research Associate Intern jobs?

Cities in Quebec with the most Clinical Research Associate Intern job openings:

Clinical Research Associate Intern jobs near you
Infographic showing various Clinical Research Associate Intern job openings in Quebec as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 15% Part Time, and 7% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $65,620 per year, or $31.5 per hour.

Clinical Research Associate

Translational Research in Oncology

Montreal, QC • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Posted 8 days ago

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 academic 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 Canada. 

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: 

  • A minimum of 2 years of monitoring experience in oncology trials
  • Fluent in English and French
  • Experience monitoring phase 1 trials 
  • An advanced level of oncology knowledge
  • 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 both English and French 

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 premiums paid by TRIO 
  • Flexible working hours
  • Monthly internet allowance 
  • Up to 5% RRSP Matching Program 
Pay Range $105,000.00 to $140,000.00 annually - Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.
 

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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