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Clinical Research Associate Manager Jobs in Quebec

In this role, you will collaborate with cross-functional teams, including clinical research associates (CRAs), data managers, and regulatory personnel, to deliver high-quality clinical data while ...

Oversees and tracks clinical research-related payments. Payment reconciliation at study closeout ... Manages country deliverables, timelines and results for assigned protocols to meet country ...

Oversees and tracks clinical research-related payments. Payment reconciliation at study closeout ... Manages country deliverables, timelines and results for assigned protocols to meet country ...

Oversight and tracking of clinical research-related payments. * Payment reconciliation at study ... MANAGEMENT and QUALITY OVERSIGHT: * Responsible for managing country deliverables, timelines, and ...

Minimum 1 - 2 years in Clinical Research or relevant healthcare experience * Completed job training (office management, administration, finance, health care preferred) or B.A./B.S. (Life Science ...

... we research, manufacture, and deliver innovative medicines to help people live longer, fuller ... Associate's degree & 10 years of clinical execution experience OR * High school diploma / GED & 12 ...

Showing results 21-40

Clinical Research Associate Manager information

What is a clinical research associate manager?

A Clinical Research Associate Manager is a professional responsible for overseeing and managing a team of Clinical Research Associates (CRAs) who monitor clinical trials to ensure they are conducted according to protocols, regulatory requirements, and good clinical practice. They coordinate trial activities, provide guidance and training to CRAs, and serve as a liaison between the research team, sponsors, and regulatory bodies. Their role is crucial for maintaining the quality and integrity of clinical research studies.

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

To thrive as a Clinical Research Associate Manager, you need expertise in clinical trial management, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and project management certifications like PMP are commonly required. Strong leadership, communication, and problem-solving skills help you effectively oversee teams and ensure adherence to protocols. These skills are crucial for ensuring high-quality research, regulatory compliance, and successful project delivery in clinical studies.

What are some common challenges faced by clinical research associate managers when overseeing multiple clinical trials simultaneously?

Clinical Research Associate Managers often face the challenge of balancing oversight across several ongoing clinical trials, each with unique protocols and site requirements. Managing competing deadlines, ensuring regulatory compliance, and maintaining clear communication across diverse teams are critical aspects of the role. Effective prioritization, strong organizational skills, and proactive risk management are essential to navigate these complexities and ensure trial success. Collaboration with CRAs, investigators, and cross-functional departments helps in addressing site issues promptly and maintaining study quality.

Is it hard to get a clinical research associate manager job?

Securing a clinical research associate manager position can be competitive, often requiring several years of experience in clinical research, strong leadership skills, and relevant certifications such as CCRP or RAC. Candidates with a background in clinical operations, good understanding of regulatory requirements, and proficiency with trial management tools tend to have better prospects.

What are popular job titles related to Clinical Research Associate Manager jobs in Quebec?

For Clinical Research Associate Manager jobs in Quebec, the most frequently searched job titles are:

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

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

Infographic showing various Clinical Research Associate 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.

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

Kirkland, QC • On-site

IQVIA
Health Care and Social Assistance • 10K+ employees

Full-time

Re-posted 7 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

63rd of 226 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 $74,700.00 - $124,500.00. 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 $74,700.00 - $124,500.00. 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

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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