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Clinical Research Associate Manager Jobs in Quebec

Senior Clinical Research Associate

Montreal, QC ยท 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 II

Montreal, QC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. * Strong organizational and communication ...

$16.25 - $20.30/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

As a Management Services Organization (MSO), Spire provides the infrastructure for administrative ... The Clinical Researcher will develop, implement, and coordinate research and administrative ...

Study Start Up CRA

Montreal, QC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Associate (Study Start Up) ICON is a global healthcare intelligence and clinical ... Collaborates with the SSO Study Start Up Manager, the SSO Study Start Up Team Lead and global study ...

Clinical Research Nurse

Montreal, QC ยท On-site

  • Medical

  • Dental

  • Vision

  • PTO

The Clinical Research Nurse will execute tasks performed in compliance with study protocol, Good ... Capable of managing multiple conflicting priorities. * Relevant industry experience a plus.

Research Associate

Montreal, QC ยท On-site

CA$35.37/hr

We are seeking a highly skilled and motivated Research Associate to lead the technical development ... Codebase Management: Overseeing the continued development and maintenance of a large, specialized ...

Research Associate

Montreal, QC ยท On-site

CA$35.37/hr

We are seeking a highly skilled and motivated Research Associate to lead the technical development ... Codebase Management: Overseeing the continued development and maintenance of a large, specialized ...

About the role The Clinical Research Technician will work with Clinic teams to execute clinical ... Other tasks as assigned by management. What you'll need to succeed * High School Diploma or/and ...

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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:

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.

Senior Clinical Research Associate

Icon plc

Montreal, QC โ€ข On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 7 hours ago


Job description

Senior CRA (Home-Based) - Canada

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


Overview:

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

DESCRIPTION DU POSTE

ICON plc est une organisation de recherche clinique et d'intelligence en soins de sante de premier plan a l'echelle mondiale. De la molecule a la medecine, nous faisons progresser la recherche clinique en offrant des services externalises aux entreprises pharmaceutiques, biotechnologiques et d'equipement medical, ainsi qu'aux organismes gouvernementaux et de sante publique.

En maintenant nos patients au centre de toutes nos activites, nous aidons a accelerer le developpement des medicaments et des dispositifs qui sauvent des vies et ameliorent la qualite de vie.

Nos employes sont au cur de notre culture et constituent la force motrice de notre succes. Les employes d'ICON ont pour mission de reussir et leur passion garantit que nous faisons bien notre travail.

Responsibilities:

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 in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

Responsabilites

En tant qu'associe(e) de recherche clinique (ARC), vous surveillerez les progres des etudes cliniques aux centres d'etude ou a distance, et vous vous assurerez que les etudes cliniques sont menees, documentees et signalees conformement au protocole, aux procedures operationnelles normalisees (PON), aux bonnes pratiques cliniques (BPC) elaborees par la Conference internationale sur l'harmonisation (CIH) et a toutes les exigences reglementaires applicables.

Qualifications:

What do you need to have?

  • Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role

  • 1+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role; 3+ years is required for a level 3

  • ONCOLOGY MONITORING EXPERIENCE PREFERRED

  • ABILITY TO TRAVEL 70%

  • Knowledge of ICH and local regulatory authority regulations regarding drug trials


To qualify, applicants must be legally authorized to work in the United States or Canada, and should not require, now or in the future, sponsorship for employment visa status

Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.


If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Qualifications

Que devez-vous avoir?

  • Avoir un baccalaureat ou son equivalent international dans un domaine clinique, scientifique ou lie a la sante d'un etablissement accredite; etre un professionnel de la sante autorise (c.-a-d., une infirmiere diplomee); ou avoir une experience de travail equivalente

  • Un minimum de 1ans d'experience en surveillance clinique ou une combinaison equivalente d'education et d'experience pour le role de niveau2; plus de 3ans pour le role de niveau3

  • BILINGUE (ANGLAIS/FRANCAIS) REQUIS

  • EXPERIENCE DE SUIVI EN ONCOLOGIE PREFERABLE

  • CAPACITE DE VOYAGER DE 70%

  • Connaissance des regles de la CIH et des autorites de reglementation locales relatives aux etudes sur les medicaments


Pour etre admissibles, les candidats doivent etre legalement autorises a travailler aux Etats-Unis ou au Canada, et ne doivent pas avoir besoin de parrainage pour leur visa d'emploi maintenant ou a l'avenir

Les avantages de travailler pour ICON:
Notre succes depend des connaissances, des capacites et de la qualite de nos employes. C'est pourquoi nous nous engageons a developper nos employes a l'aide d'une culture d'apprentissage continu - une culture ou nous vous mettons au defi de travailler avec engagement et ou chaque experience contribue a votre developpement professionnel.
Chez ICON, notre objectif est de vous fournir une gamme complete et competitive de recompenses comprenant, non seulement un excellent salaire de base, mais aussi un large eventail de programmes de remuneration et de reconnaissances. De plus, nous offrons des avantages sociaux, des politiques de soutien et des initiatives de bien-etre de premiere qualite, afin de vous soutenir, vous et votre famille, a toutes les etapes de votre carriere, maintenant et a l'avenir.
ICON, y compris ses filiales, est un employeur inclusif qui offre des chances egales d'emploi et qui s'engage a offrir un milieu de travail exempt de discrimination et de harcelement. Tous les candidats qualifies recevront une consideration egale pour l'emploi sans egard a la race, la couleur, la religion, le sexe, l'orientation sexuelle, l'identite de genre, l'origine nationale, le handicap ou le statut d'ancien combattant protege.


Si, en raison d'un probleme de sante ou d'un handicap, vous avez besoin d'un accommodement raisonnable pour toute partie du processus de candidature, ou afin d'executer les fonctions essentielles d'un poste, veuillez nous en aviser.

#LI-REMOTE


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply