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Clinical Research Data Manager Jobs in Quebec (NOW HIRING)

Research/Data Generation Support: * Supports Gilead clinical operations through site/investigator ... Excellent project management ability and organizational skills, including the management of ...

Manage LSOM and LSOM vendor performance to guarantee high-quality study execution, serving as the ... Experience at, or oversight of, clinical research vendors (CRO's, central labs, imaging vendors ...

... human performance data; collaborate with military and multidisciplinary partners; and brief ... Clinical Exercise Physiologist (CEP) certification or National Strength and Conditioning ...

... human performance data; collaborate with military and multidisciplinary partners; and brief ... Clinical Exercise Physiologist (CEP) certification or National Strength and Conditioning ...

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Clinical Research Data Manager information

See Quebec salary details

$11

$38

$66

How much do clinical research data manager jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical research data manager in Quebec is $38.73, according to ZipRecruiter salary data. Most workers in this role earn between $22.60 and $52.40 per hour, depending on experience, location, and employer.

What is a clinical research data manager?

A Clinical Research Data Manager is a professional responsible for collecting, organizing, and managing the data generated during clinical trials and research studies. They ensure that the data is accurate, complete, and complies with regulatory standards. Their work is crucial for the integrity of clinical research, as it allows researchers to draw valid conclusions from the study. Data managers work closely with clinical teams, statisticians, and regulatory bodies to maintain high-quality data throughout the research process.

What are some common challenges faced by clinical research data managers during multi-site trials?

Clinical Research Data Managers often encounter challenges coordinating data collection across multiple research sites, such as ensuring consistent data entry, handling discrepancies, and maintaining data quality standards. Effective communication with site staff and timely resolution of data queries are essential to minimize delays and errors. Utilizing robust electronic data capture (EDC) systems and standardized procedures helps, but proactive problem-solving and attention to detail remain crucial for success in this role.

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

To thrive as a Clinical Research Data Manager, you need a solid background in life sciences, data management principles, and experience with clinical trial processes, often backed by a relevant bachelor's degree. Proficiency in electronic data capture (EDC) systems, database management tools like SQL, and familiarity with regulatory standards such as GCP are essential. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration across research teams. These skills are crucial for maintaining high-quality, compliant data that support successful clinical trials and regulatory submissions.

What is the difference between Clinical Research Data Manager vs Clinical Research Coordinator?

AspectClinical Research Data ManagerClinical Research Coordinator
Primary RoleOversees data collection, management, and quality control of clinical trial data.Coordinates daily trial activities, patient recruitment, and site management.
Required SkillsData management, database systems, regulatory compliance.Patient interaction, study protocol adherence, site coordination.
Work EnvironmentData centers, clinical trial sites, research organizations.Clinical sites, hospitals, research facilities.
Common CertificationsCDMP, SAS, or related data management certifications.GCP certification, clinical trial training.

While both roles support clinical research, the Clinical Research Data Manager focuses on data integrity and management, whereas the Clinical Research Coordinator handles trial operations and participant coordination. Understanding these differences helps in choosing the right career path or job search focus.

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

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

What cities in Quebec are hiring for Clinical Research Data Manager jobs?

Cities in Quebec with the most Clinical Research Data Manager job openings:

Infographic showing various Clinical Research Data Manager job openings in Quebec as of August 2026, with employment types broken down into 69% Full Time, 20% Part Time, and 11% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $80,551 per year, or $38.7 per hour.

Senior Clinical Project Manager, Oncology, IQVIA Biotech

IQVIA

Kirkland, QC • On-site

Full-time

Posted 26 days ago


Key responsibilities

  • Lead the planning and execution of multi-regional clinical studies, ensuring speed, quality, and cost optimization.

  • Serve as the primary point of contact for clients, fostering strong relationships and customer satisfaction.

  • Monitor project progress, manage risks, and resolve issues proactively.


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services


Job description

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

We are seeking a Senior Clinical Project Manager with proven experience in Oncology clinical trials to join IQVIA Biotech. This role is ideal for a seasoned project management professional who thrives in a fast-paced environment and is passionate about advancing therapies in the Immuno-Oncology space. You will leverage your expertise to lead complex, multi-regional studies and ensure operational excellence while building strong client relationships.

Overview
As a Senior Clinical Project Manager at IQVIA Biotech, you'll play a critical role in accelerating the delivery of clinical trials and improving patient lives by bringing new therapies to market faster. You will lead core project teams, ensuring successful execution of clinical studies in alignment with contractual requirements, SOPs, and regulatory standards. This role combines strategic leadership, operational excellence, and customer engagement to deliver high-quality results.

Key Responsibilities

  • Lead bid defense presentations and contribute to study strategy development.

  • Develop and implement integrated study management plans.

  • Oversee planning and execution of medium to large, multi-regional clinical studies, ensuring speed, quality, and cost optimization.

  • Serve as the primary point of contact for clients, fostering strong relationships and customer satisfaction.

  • Build and lead cross-functional teams, driving collaboration and milestone achievement.

  • Monitor project progress, manage risks, and resolve issues proactively.

  • Ensure compliance with ICH GCP, local regulations, and company processes.

  • Manage project financials, including forecasting, scope changes, and revenue acceleration opportunities.

  • Mentor and support team members, promoting continuous improvement and knowledge sharing.

Qualifications

  • Bachelor's degree in Life Sciences or related field.

  • 7+ years of clinical research experience, including 4+ years in project management.

  • Strong knowledge of clinical trial conduct, regulatory requirements, and therapeutic areas.

  • Excellent leadership, communication, and negotiation skills.

  • Proven ability to manage complex projects across geographies and functions.

  • Proficiency in MS Office and project management tools.

IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de sante pour les secteurs des sciences de la vie et de la sante. IQVIA se consacre a accelerer le developpement et la commercialisation de traitements medicaux innovants pour aider a ameliorer les resultats des patients et la sante de la population dans le monde entier. Pour en savoir plus, visitez https://jobs.iqvia.com

IQVIA est fiere d'etre un employeur souscrivant au principe de l'egalite d'acces a l'emploi. Tous les candidats qualifies seront pris en consideration pour un emploi sans egard a la race, la couleur, la religion, le sexe, l'orientation sexuelle, l'identite de genre, l'origine nationale, le handicap, l'age, l'etat matrimonial ou tout autre statut protege par la loi applicable. Des mesures d'adaptation pour les candidats handicapes sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui necessite une mesure d'adaptation, nous vous encourageons a contacter notre equipe d'acquisition de talents au workday_recruiting@iqvia.com, afin qu'IQVIA puisse soutenir votre participation au processus de recrutement.

IQVIA s'engage a faire preuve d'integrite dans son processus de recrutement et applique une politique de tolerance zero en matiere de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent etre veridiques et completes. Toute fausse declaration, presentation trompeuse ou omission importante au cours du processus de recrutement entrainera la disqualification immediate de votre candidature, ou la cessation d'emploi si elle est decouverte ulterieurement, conformement aux lois applicables. Nous apprecions votre honnetete et votre professionnalisme.

Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre equipe de recrutement a selectionner ou a evaluer les candidatures, et non pas pour remplacer la prise des decisions par les membres de notre equipe.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: workday_recruiting@iqvia.com, so that IQVIA can support your participation in the recruitment process.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making.

La fourchette salariale de base potentielle pour ce poste, annualisee, est de $111,800.00 - $149,000.00. Le salaire de base reel offert peut varier selon plusieurs facteurs, notamment les qualifications liees a l'emploi telles que les connaissances, les competences, la formation et l'experience; l'emplacement; et/ou l'horaire (temps plein ou temps partiel). Selon le poste offert, des regimes d'incitation, des primes et/ou d'autres formes de remuneration peuvent etre proposes, en plus d'une gamme d'avantages sociaux lies a la sante, au bien-etre et/ou d'autres benefices.The potential base pay range for this role, when annualized, is $111,800.00 - $149,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US