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Contract Clinical Research Associate Jobs in Quebec

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Clinical Research Associate

Montreal, QC · On-site

Clinical Research Associate - Montreal, Canada - Diabetes and Obesity ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

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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

Montreal, QC

Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

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Clinical research associate II

Montreal, QC

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 ...

New

Mcgill

Research Associate

Montreal, QC

CA$35.37/hr

If you are an active McGill employee (ie: currently in an active contract or position at McGill ... Research Associate - Canada Excellence Research Chair in Metabolism and the Brain (CERC M&B ...

Mcgill

Research Associate

Montreal, QC · On-site

CA$35.37/hr

If you are an active McGill employee (ie: currently in an active contract or position at McGill ... Research Associate - Canada Excellence Research Chair in Metabolism and the Brain (CERC M&B ...

Mcgill

Research Associate

Montreal, QC

CA$35.37/hr

If you are an active McGill employee (ie: currently in an active contract or position at McGill ... The Research Associate will work in collaboration with the Research Supervisor, to develop and ...

Mcgill

Research Associate

Montreal, QC

CA$35.37/hr

If you are an active McGill employee (ie: currently in an active contract or position at McGill ... The Research Associate will work in collaboration with the Research Supervisor, to develop and ...

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Showing results 1-20

All JobsContract Clinical Research Associate JobsContract Clinical Research Associate Jobs in Quebec

Contract Clinical Research Associate information

See Quebec salary details

$12

$44

$92

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

As of Aug 2, 2026, the average hourly pay for contract clinical research associate in Quebec is $44.58, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $54.33 per hour, depending on experience, location, and employer.

What are some of the unique challenges faced by Contract Clinical Research Associates compared to permanent employees?

Contract Clinical Research Associates often need to quickly adapt to new study protocols, sponsor requirements, and team dynamics since they may work on multiple projects for different organizations. This can mean a faster onboarding process and the need to build rapport with new colleagues and site staff efficiently. Additionally, contract CRAs must be highly organized to manage shifting assignments and maintain compliance across different trial sites, as well as keep up with varying documentation standards. While this variety can be rewarding, it can also present challenges in terms of consistency and long-term project ownership.

What are Contract Clinical Research Associates?

Contract Clinical Research Associates (CRAs) are professionals who monitor clinical trials on behalf of pharmaceutical companies, contract research organizations (CROs), or other sponsors, but work on a contract or freelance basis rather than as permanent employees. Their primary responsibilities include ensuring that trials are conducted according to regulatory guidelines, monitoring data accuracy, and verifying that patient rights and safety are protected. Contract CRAs may work on multiple projects for different clients and often enjoy more flexibility in their schedules and work locations. This role requires strong organizational skills, knowledge of Good Clinical Practice (GCP), and the ability to travel to clinical sites.

What are the key skills and qualifications needed to thrive as a Contract Clinical Research Associate, and why are they important?

To thrive as a Contract Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP and ICH), and typically a degree in life sciences or related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are highly valued. Strong attention to detail, organizational skills, and effective communication help build productive site relationships and ensure compliance. These skills are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting successful clinical trial outcomes.

What is the difference between Contract Clinical Research Associate vs Clinical Research Associate?

AspectContract Clinical Research AssociateClinical Research Associate
CredentialsTypically requires a degree in life sciences and relevant certificationsSame as Contract CRA, often with additional experience
Work EnvironmentTemporary, project-based assignments often with multiple sponsorsFull-time employment with a single organization or sponsor
Employer & Industry UsageUsed by CROs and pharma companies for short-term projectsCommonly employed directly by pharmaceutical companies or CROs
Search & Comparison IntentOften compared for flexibility and contract work benefitsViewed as a permanent role with career growth

In summary, Contract Clinical Research Associates work on temporary, project-specific basis, often with multiple sponsors, offering flexibility. Clinical Research Associates typically hold full-time roles within a single organization, providing stability and career development opportunities.

What are popular job titles related to Contract Clinical Research Associate jobs in Quebec? For Contract Clinical Research Associate jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Contract Clinical Research Associate jobs in Quebec look for? The top searched job categories for Contract Clinical Research Associate jobs in Quebec are:
What cities in Quebec are hiring for Contract Clinical Research Associate jobs? Cities in Quebec with the most Contract Clinical Research Associate job openings:
Contract Clinical Research Associate jobs near you
Infographic showing various Contract Clinical Research Associate job openings in Quebec as of July 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Contract. Highlights an 90% In-person, 5% Hybrid, and 5% Remote job distribution, with an average salary of $92,733 per year, or $44.6 per hour.

Senior Clinical Research Associate

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Montreal, QC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 14 days ago

Job description

Senior Clinical Research Associate - Cardio Device - Canada

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


Senior Clinical Research Associate - Cardio

To support 1study in the cardiovascular/electrophysiology medical device space. Indication is A-fib.

  • Candidates must have complex cardiac experience within the past 5 years, preferably in electrophysiology and / or devices.

3 years of monitoring experience required.

A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.

Candidates must have/ be:

  • In-depth knowledge of FDA regulations and ICH/GCP guidelines.

  • Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.

  • Fluent in French and English.

  • Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.

  • Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.

  • Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.

  • Ability to work independently and manage multiple priorities in a dynamic environment.

  • A well-executed plan for communication with the study teams and sites.

  • Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their reports.

  • Located in the Montreal area. Ability to cover up to 60% regional travel.


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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