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Clinical Research Associate Jobs in Quebec (NOW HIRING)

Train Research Associates on sample preparation and analytical techniques * Provide scientific ... stage clinical trials. The Company operates globally with facilities located in Canada, USA ...

About The Role The Associate Scientist is the right-hand help for the senior scientist. As such ... The requirement to have study protocols, designs and clinical research documents written and ...

CA$75K/yr

About Charles River Charles River is an early-stage contract research organization (CRO). We have ... Charles River also provides a suite of products and services to support our clients' clinical ...

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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 Aug 9, 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.

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 such as a life sciences or healthcare-related field, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve job prospects, but entry may be challenging for those without relevant qualifications or experience.

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 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 the chance to contribute to medical advancements, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in healthcare and research.

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.
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:
Infographic showing various Clinical Research Associate job openings in Quebec as of July 2026, with employment types broken down into 1% As Needed, 73% Full Time, 24% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $81,357 per year, or $39.1 per hour.

Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech

IQVIA

Quebec, QC • On-site

Full-time

Re-posted yesterday


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 223 rated it services


Job description

Attache de recherche clinique II

IQVIA Biotech est une CRO offrant une gamme complete de services et concue pour accompagner les promoteurs de biotechnologies. Forte de plus de 25 ans d'experience, elle propose des solutions agiles et adaptees aux besoins therapeutiques, ainsi que des partenariats de confiance qui contribuent a accelerer l'acces des patients a des traitements innovants.

IQVIA Biotech est a la recherche d'un ARC II experimente en surveillance d'essais cliniques en oncologie. Ce poste, base a domicile dans l'est du Canada, necessite la maitrise du francais et de l'anglais.

Apercu du poste

  • L'ARC II est responsable de la surveillance des essais cliniques de phase I a IV afin d'assurer la conformite aux protocoles, aux BPC/ICH et aux exigences reglementaires. Elle gere les activites des sites, du debut a la cloture.
  • Principales responsabilites
  • Effectuer les visites de selection, d'initiation, de suivi et de cloture des sites
  • Former le personnel des sites aux protocoles d'etude, aux systemes EDC et aux exigences de l'etude
  • Assurer la qualite de la documentation source, l'integrite des donnees et la resolution rapide des requetes
  • Superviser la responsabilite des enqueteurs et la collecte des documents reglementaires
  • Etre l'interlocuteur principal du site et maintenir une communication reguliere
  • Preparer les rapports de suivi conformement aux procedures operationnelles standard (SOP) et aux echeanciers
  • Soutenir les reunions des enqueteurs et collaborer avec les coordonnateurs principaux d'etude/ARC

Diplomes et experience

  • Bilingue francais-anglais (obligatoire)
  • Baccalaureat requis. De preference en sciences de la vie ou dans une discipline connexe
  • Une combinaison equivalente de formation et d'experience peut etre acceptee au lieu du diplome
  • Au moins 1 an d'experience en suivi sur place (requis)
  • Disponibilite pour des deplacements a hauteur de 65 a 70 %

Clinical Research Associate II

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.

IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology monitoring experience. This role is homebased in Eastern Canada and requires fluency in both French and English.

Overview

The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from start-up through close-out.

Key Responsibilities

  • Conduct site selection, initiation, monitoring, and close-out visits
  • Train site personnel on study protocols, EDC systems, and study requirements
  • Ensure high-quality source documentation, data integrity, and timely query resolution
  • Oversee IP accountability and regulatory document collection
  • Serve as the primary site contact and maintain regular communication
  • Prepare monitoring reports following Standard Operating Procedures and timelines
  • Support investigator meetings and collaborate with CTMs/Lead CRAs

Qualifications

  • Bilingual in French and English (Required).
  • Bachelor's Degree required. Preference in life sciences or related discipline. Equivalent combination of education, training and experience may be accepted in lieu of degree.
  • At least 1 year of onsite monitoring experience (Required)
  • Ability to travel 65-70%

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 $72,100.00 - $134,000.00. 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 $72,100.00 - $134,000.00. 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