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Clinical Research Monitor Jobs in Quebec (NOW HIRING)

The Clinical Research Nurse will execute tasks performed in compliance with study protocol, Good ... Monitor, document and/or follow-up on participant adverse events. * Maintain and advocate a high ...

Senior Clinical Research Associate

Montreal, QC · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Senior Clinical Research Associate

Montreal, QC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Clinical Research Associate

Montreal, QC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... Your role will involve delivering clinical trial monitoring work to a high standard, working ...

Clinical research associate II

Montreal, QC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: * Conducting site qualification ...

Research Assistant 1

Montreal, QC · On-site

CA$30.54/hr

... monitor questionnaire completion (e.g. REDCap), and coordinate biospecimen collection. (v) Work jointly with the Clinical Research Unit (CRU) to identify and refer eligible patients for clinical ...

Research Assistant 1

Montreal, QC · On-site

CA$30.54/hr

... monitor questionnaire completion (e.g. REDCap), and coordinate biospecimen collection. (v) Work jointly with the Clinical Research Unit (CRU) to identify and refer eligible patients for clinical ...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the ... Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i ...

Start-up Administrator

Montreal, QC · On-site

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Monitor financial activity for clinical trials and ensure payments are received by the sponsor and ... Provide backup support to other administrative or research support staff within area of ...

New

Start-up Administrator

Montreal, QC · On-site

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Monitor financial activity for clinical trials and ensure payments are received by the sponsor and ... Provide backup support to other administrative or research support staff within area of ...

New

Study Start Up CRA

Montreal, QC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

An experienced Clinical Research Associate with a minimum of 2 years of on-site monitoring experience. * Knowledgeable in clinical trial processes, regulatory requirements, and ICH-GCP guidelines.

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Showing results 1-20

Clinical Research Monitor information

See Quebec salary details

$22.5K

$81K

$127K

How much do clinical research monitor jobs pay per year?

As of Aug 13, 2026, the average yearly pay for clinical research monitor in Quebec is $80,990.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,000.00 and $105,000.00 per year, depending on experience, location, and employer.

What is a clinical research monitor?

A clinical research monitor, also called a clinical research associate, oversees the operations of a clinical trial to ensure that it meets all safety and governmental regulations. As a clinical research monitor, your job duties include traveling to testing sites, inspecting the procedures, documenting results from the trial, and verifying that all collected data is accurate and verified. Your primary responsibility is to make sure the testing is conducted safely and within industry and governmental guidelines.

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

To thrive as a Clinical Research Monitor, you need a solid understanding of clinical trial protocols, regulatory compliance (such as GCP), and a degree in life sciences or a related field. Familiarity with electronic data capture systems, trial management software, and certifications like ACRP or SOCRA are highly valued. Excellent organizational skills, attention to detail, and effective communication are essential soft skills for managing site relationships and ensuring protocol adherence. These competencies are crucial for safeguarding data integrity, patient safety, and regulatory compliance throughout the clinical trial process.

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

AspectClinical Research MonitorClinical Research Associate
CertificationsOften required or preferred certifications like CCRP or CCRASimilar certifications such as CCRP or CCRA are common
Work EnvironmentMonitoring visits at sites, reviewing data, ensuring complianceSite visits, data collection, and regulatory documentation
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms

Both roles involve overseeing clinical trial activities, ensuring compliance, and maintaining data integrity. While the titles are often used interchangeably, the term 'Clinical Research Monitor' emphasizes the monitoring aspect, whereas 'Clinical Research Associate' may encompass broader responsibilities in clinical trial management. Both roles require similar certifications and work in comparable environments within the industry.

What does a clinical research monitor do in clinical research?

A clinical research monitor oversees the progress of clinical trials to ensure compliance with regulatory requirements and study protocols. They review data, conduct site visits, and verify that trial procedures are followed correctly, often using electronic data capture systems. Their role is essential for maintaining data integrity and participant safety throughout the study.

What are some common challenges clinical research monitors face when overseeing multiple study sites?

Clinical Research Monitors often encounter challenges such as managing varying levels of compliance across different sites, coordinating communication between site staff and sponsors, and ensuring timely data collection and reporting. Travel between sites and adapting to diverse protocols or site-specific processes can also present logistical hurdles. Successful monitors develop strong organizational skills, maintain meticulous documentation, and build collaborative relationships with site teams to navigate these challenges effectively.
What are popular job titles related to Clinical Research Monitor jobs in Quebec? For Clinical Research Monitor jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Clinical Research Monitor jobs in Quebec look for? The top searched job categories for Clinical Research Monitor jobs in Quebec are:
Infographic showing various Clinical Research Monitor 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 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $80,990 per year, or $38.9 per hour.

Full-time

Medical, Dental, Vision, PTO

Re-posted 11 days ago


Altasciences rating

7.6

Company rating: 7.6 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

59th of 120 rated laboratories


Job description

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.

We are better together and together We Are Altasciences.

About The Role

The Clinical Research Nurse will oversee the safety and consent of clinical trial participants during study conduct and the maintenance of safety equipment. 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 scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records.

  • Ensure the confidentiality of clinical trial participants and sponsors is respected.

  • Perform clinical trial activities including but not limited to, continuous safety monitoring, safety assessments, Investigational Product (IP) administration and catheter installation.

  • Monitor, document and/or follow-up on participant adverse events.

  • Maintain and advocate a high level of patient care, quality, and safety within the department.

  • May assist in study related consenting with participant screenings.

  • Provide feedback, where necessary, to appropriate team members of study progress.

  • Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.

  • May train employees on clinical trial activities associated to their job's needs.

  • Other tasks as assigned by management.

What You'll Need to Succeed

  • DEC from accredited Registered Nurse program required

  • Permit from the Ordre des infirmiers et infirmieres du Quebec (OIIQ) required.

  • Good communication in French and English.

  • Customer service focused.

  • Able to work in fast-paced environment.

  • Knowledge of the Microsoft suite

  • Excellent verbal and written communication skills.

  • Well-developed interpersonal skills are required.

  • Personal/professional integrity and proven discretion in handling confidential information.

  • Capable of managing multiple conflicting priorities.

  • Relevant industry experience a plus.

Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of Clinical Research Nurse including, but not limited to, for the following reasons:

  • The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.

What We Offer

  • Full time position (37,5 hours/week).

  • Availability every other weekend is required.

  • Day, evening or night shift (no shift rotation).

  • 6 to 8 weeks of theory and practical training on the day shift.

  • On site position at our Montreal site (1200 Beaumont).

  • Accessible by public transportation (Metro L' Acadie), Free parking for employees.

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences' Benefits Package Includes:

  • Health/Dental/Vision Insurance Plans

  • RRSP with Employer Match

  • Paid Vacation and Holidays

  • Paid Sick and Bereavement Leave

  • Employee Assistance & Telehealth Programs

Altasciences' Incentive Programs Include:

  • Training & Development Programs

  • Employee Referral Bonus Program

  • Annual Performance Reviews

#LI-JG1

MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!


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