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Clinical Data Manager Jobs in Quebec (NOW HIRING)

Medfar

Data Transfer Team Lead

Montreal, QC · Hybrid

Company Description MEDFAR Clinical Solutions was founded in 2010 by two aeronautical engineers who ... Main Responsibilities Team Management & Leadership * Supervise, coach, and motivate the data ...

ASICC-MED

Dental Assistant

Montreal, QC · On-site

CA$28 - CA$32/hr

... Managing the sterilization and decontamination of instruments Take dental X-rays (according to ... clinical data, as needed. REQUIRED QUALIFICATIONS: Diploma of Vocational Studies (DEP) in Dental ...

ASICC-MED

Dental Assistant

Montreal, QC · On-site

CA$28 - CA$32/hr

... Managing the sterilization and decontamination of instruments Take dental X-rays (according to ... clinical data, as needed. REQUIRED QUALIFICATIONS: Diploma of Vocational Studies (DEP) in Dental ...

ASICC-MED

Dental Assistant

Montreal, QC · On-site

CA$28 - CA$32/hr

... Managing the sterilization and decontamination of instruments Take dental X-rays (according to ... clinical data, as needed. REQUIRED QUALIFICATIONS: Diploma of Vocational Studies (DEP) in Dental ...

ASICC-MED

Dental Assistant

Montreal, QC · On-site

CA$28 - CA$32/hr

... Managing the sterilization and decontamination of instruments Take dental X-rays (according to ... clinical data, as needed. REQUIRED QUALIFICATIONS: Diploma of Vocational Studies (DEP) in Dental ...

ASICC-MED

Dental Assistant

Montreal, QC · On-site

CA$28 - CA$32/hr

... Managing the sterilization and decontamination of instruments Take dental X-rays (according to ... clinical data, as needed. REQUIRED QUALIFICATIONS: Diploma of Vocational Studies (DEP) in Dental ...

ASICC-MED

Dental Assistant

Montreal, QC · On-site

CA$28 - CA$32/hr

... Managing the sterilization and decontamination of instruments Take dental X-rays (according to ... clinical data, as needed. REQUIRED QUALIFICATIONS: Diploma of Vocational Studies (DEP) in Dental ...

CHSLD de Laval

Auxiliary nurse

Laval, QC · On-site

Contribute to the assessment of residents' health status by collecting clinical data, observing ... Provide palliative care to residents at the end of life, ensuring their comfort, managing pain and ...

CHSLD de Laval

Auxiliary nurse

Laval, QC · On-site

Contribute to the assessment of residents' health status by collecting clinical data, observing ... Providing palliative care to residents at the end of their lives, ensuring their comfort, managing ...

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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All JobsClinical Data JobsClinical Data Manager JobsClinical Data Manager Jobs in Quebec

Clinical Data Manager information

See Quebec salary details

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How much do clinical data manager jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical data manager in Quebec is $52.35, according to ZipRecruiter salary data. Most workers in this role earn between $41.11 and $62.26 per hour, depending on experience, location, and employer.

What does a clinical data manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

What does a clinical data manager do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

What are the key skills and qualifications needed to thrive as a clinical data manager?

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What are some common challenges clinical data managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

How much do clinical data managers make in the US?

Clinical data managers in the US typically earn between $70,000 and $110,000 annually, with salaries varying based on experience, education, and location. Entry-level positions may start around $60,000, while experienced professionals with specialized skills can earn over $120,000. Certifications in data management and proficiency with electronic data capture systems can also influence salary levels.
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For Clinical Data Manager jobs in Quebec, the most frequently searched job titles are:

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Clinical Data Manager jobs near you
Infographic showing various Clinical Data Manager job openings in Quebec as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 81% Physical, 3% Hybrid, and 16% Remote job distribution, with an average salary of $108,878 per year, or $52.3 per hour.

Manager, Clinical Quality Control Department

Altasciences

Montreal, QC • Hybrid

Full-time

Medical, Dental, Vision, PTO

Re-posted yesterday

Altasciences rating

7.6

Company rating: 7.6 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

61st of 121 rated laboratories

Job description

About The Role

The Manager, Clinical Quality Control Department is responsible for the management of the Quality Systems team, ensuring the quality of clinical trial data and the efficiency and completion of quality related tasks. The Manager, Clinical Quality Control Department will ensure tasks performed are conducted within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).

What You'll Do Here

  • Management of the Quality Systems team, including but not limited to, PTO management, timesheet approval, on-going and yearly performance reviews, employee hiring, disciplinary actions and termination.

  • Perform, direct and/or oversee the training of the Quality Systems team.

  • Proactively assess learning opportunities for the Quality Systems team.

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

  • Maintain and advocate a high level of quality and customer service within the department.

  • Participate in sponsor/regulatory audits, respond to and/or complete pre-site audit questionnaires and audit reports.

  • Review quality inputs/deviations, track trends and evaluate the QC process and risk mitigation; escalate as required.

  • Implement quality initiatives and process improvements within the department.

  • Monitor clinical trial timelines to ensure clinical trial data milestones are met related to data entry, query tracking and resolution, and deviation management.

  • Participate in SOP revisions.

  • Perform and/or ensure the training on external databases.

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

  • Hold meetings to communicate clinical trial needs and/or departmental objectives.

What You'll Need to Succeed

  • College or University Degree completed

  • Minimum of 3 years of experience in the clinical research field

  • 3 to 5 plus years related experience in management of a team

  • Microsoft suite

  • Strong computer literacy

  • Ability to read and interpret technical documents and industry specific manuals. Ability to write advanced reports and correspondence.

  • Bilingual proficiency in English/French

  • Excellent verbal and written communication skills.

  • Well-developed interpersonal skills are required.

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

  • Ability to develop strong trusting relationships in order to gain support and achieve results.

  • Must be self-directed, motivated, and have a willingness to take the initiative to identify and anticipate client needs and make recommendations for implementation.

  • Customer service focused.

  • Able to work in fast-paced environment with conflicting priorities.

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 Quality Control Associate 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

  • Regular full-time position; 37.5 hours a week.

  • Candidate needs to be available between 7am and 5pm.

  • Hybrid position (3 days on site, Montreal site (1200 Beaumont) - 2 days remote).

  • Needs to be available to be full time on site for the training period.

  • Accessible by metro (L'Acadie); Free parking for employees.

Altasciences offers a wide range of benefits to help employees live healthy and satisfying lives, both on and off the job.

Altasciences benefits include

  • Health/dental/vision insurance plans

  • RRSP with employer match

  • Paid vacation and statutory vacations

  • Paid sick leave and bereavement leave

  • Employee assistance and telehealth programs

Altasciences' incentive programs include

  • Training and development programs

  • Employee orientation bonus program

  • Annual performance reviews

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