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Clinical Research Associate Jobs in Quebec (NOW HIRING)

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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 ...

Altasciences

Clinical Research Nurse

Beaumont, QC

The Clinical Research Nurse will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). What You'll Do Here * Perform ...

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Senior CRA

Montreal, QC · On-site

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 ...

Mcgill

Research Associate

Montreal, QC · On-site

CA$35.37/hr

The candidate will work independently on basic research projects in the laboratory of Dr. Ruthazer at the MNI. His/her work will develop a multilevel understanding of the behavioral responses of ...

Mcgill

Clinical Research Coordinator

Montreal, QC · Hybrid

CA$33.05 - CA$40.97/hr

Serve as liaison between researchers, participants, the Clinical Research Manager and the Program Manager. Data, Sample & Regulatory Oversight * Maintain study documentation (e.g., Investigator Site ...

Mcgill

Clinical Research Coordinator

Montreal, QC · Hybrid

CA$33.05 - CA$40.97/hr

Serve as liaison between researchers, participants, the Clinical Research Manager and the Program Manager. Data, Sample & Regulatory Oversight * Maintain study documentation (e.g., Investigator Site ...

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Clinical Research Associate information

See Quebec salary details

$16

$39

$61

How much do clinical research associate jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for clinical research associate in Quebec is $39.11, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $46.39 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
More about Clinical Research Associate jobs

What are the most commonly searched types of Clinical Research jobs in Quebec?

The most popular types of Clinical Research jobs in Quebec are:

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

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

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

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

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

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

Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Quebec as of September 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $81,357 per year, or $39.1 per hour.

Clinical Research Associate

Montreal, QC • On-site

Translational Research in Oncology
See more jobs at Translational Research in Oncologyexternal

Full-time

Medical, Dental, Vision, Life, PTO

Posted 18 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 Eastern 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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