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ICR Canada - CAN

Senior Clinical Research Associate

Burlington, ON, Canada
BC, Canada
AB, Canada
Montréal, QC, Canada

On-site

Salary Range $108,576.00-$135,720.00 Are you a current ICON Employee? · Full-time

Apply on icon.wd3.myworkdayjobs.com About employer

Applications open in a new tab.

Job details

Pay: Salary Range $108,576.00-$135,720.00 Are you a current ICON Employee?
Job type: Full-time
Workplace: On-site
Experience: 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
Posting language: English · French
Posted: Oct 12, 2026

Original job description

English section of this bilingual listing.

Senior CRA / CRA II

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.

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.

Responsabilités

Qualifications:

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.

Que devez-vous avoir?

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.

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

Read the full bilingual original

Senior CRA / CRA II

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:

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.

DESCRIPTION DU POSTE

ICON plc est une organisation de recherche clinique et d’intelligence en soins de santé de premier plan à l’échelle mondiale. De la molécule à la médecine, nous faisons progresser la recherche clinique en offrant des services externalisés aux entreprises pharmaceutiques, biotechnologiques et d’équipement médical, ainsi qu’aux organismes gouvernementaux et de santé publique.

En maintenant nos patients au centre de toutes nos activités, nous aidons à accélérer le développement des médicaments et des dispositifs qui sauvent des vies et améliorent la qualité de vie.

Nos employés sont au cœur de notre culture et constituent la force motrice de notre succès. Les employés d’ICON ont pour mission de réussir et leur passion garantit que nous faisons bien notre travail.

Responsibilities:

Responsabilités

En tant qu’associé(e) de recherche clinique (ARC), vous surveillerez les progrès des études cliniques aux centres d’étude ou à distance, et vous vous assurerez que les études cliniques sont menées, documentées et signalées conformément au protocole, aux procédures opérationnelles normalisées (PON), aux bonnes pratiques cliniques (BPC) élaborées par la Conférence internationale sur l’harmonisation (CIH) et à toutes les exigences réglementaires 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

Qualifications

Que devez-vous avoir?

Avoir un baccalauréat ou son équivalent international dans un domaine clinique, scientifique ou lié à la santé d’un établissement accrédité; être un professionnel de la santé autorisé (c.-à-d., une infirmière diplômée); ou avoir une expérience de travail équivalente
Un minimum de 1 ans d’expérience en surveillance clinique ou une combinaison équivalente d’éducation et d’expérience pour le rôle de niveau 2; plus de 3 ans pour le rôle de niveau 3
BILINGUE (ANGLAIS/FRANÇAIS) REQUIS
EXPÉRIENCE DE SUIVI EN ONCOLOGIE PRÉFÉRABLE
CAPACITÉ DE VOYAGER DE 70 %
Connaissance des règles de la CIH et des autorités de réglementation locales relatives aux études sur les médicaments

Pour être admissibles, les candidats doivent être légalement autorisés à travailler aux États-Unis ou au Canada, et ne doivent pas avoir besoin de parrainage pour leur visa d’emploi maintenant ou à l’avenir

Les avantages de travailler pour ICON :
Notre succès dépend des connaissances, des capacités et de la qualité de nos employés. C’est pourquoi nous nous engageons à développer nos employés à l’aide d’une culture d’apprentissage continu – une culture où nous vous mettons au défi de travailler avec engagement et où chaque expérience contribue à votre développement professionnel.

Chez ICON, notre objectif est de vous fournir une gamme complète et compétitive de récompenses comprenant, non seulement un excellent salaire de base, mais aussi un large éventail de programmes de rémunération et de reconnaissances. De plus, nous offrons des avantages sociaux, des politiques de soutien et des initiatives de bien-être de première qualité, afin de vous soutenir, vous et votre famille, à toutes les étapes de votre carrière, maintenant et à l’avenir.

ICON, y compris ses filiales, est un employeur inclusif qui offre des chances égales d’emploi et qui s’engage à offrir un milieu de travail exempt de discrimination et de harcèlement. Tous les candidats qualifiés recevront une considération égale pour l’emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap ou le statut d’ancien combattant protégé.

Si, en raison d’un problème de santé ou d’un handicap, vous avez besoin d’un accommodement raisonnable pour toute partie du processus de candidature, ou afin d’exécuter les fonctions essentielles d’un poste, veuillez nous en aviser.

#LH-ZH1

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 request here.

Salary Range

$108,576.00-$135,720.00

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

Apply on icon.wd3.myworkdayjobs.com About employer

More about this job

Responsibilities

The Senior Clinical Research Associate will check how clinical studies are progressing at study sites or remotely. They make sure trials are run, recorded and reported according to the protocol and regulatory rules.

Requirements

Candidates need a bachelor's degree or equivalent in a scientific or health field, plus at least 3 years of clinical monitoring experience for this senior level. Knowledge of ICH and regulatory rules for drug trials and fluent English and French are required.

Skills

Clinical monitoring
ICH-GCP
Good Clinical Practice
Clinical trial protocols
Standard operating procedures (SOPs)
Regulatory compliance
Oncology
Site visits and remote monitoring
Source document verification
Clinical trial reporting
Bilingual English and French
Travel
Study coordination
Data review and quality control
Stakeholder communication

Benefits

Competitive base salary and performance related incentives
Medical, dental and vision coverage
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes
Learning and development opportunities

Keywords

Clinical Research Associate
CRA
clinical monitoring
clinical trials
ICH-GCP
good clinical practice
regulatory affairs
oncology
site monitoring
remote monitoring
SOPs
protocol compliance
drug trials
clinical research
bilingual English French
travel
CRO
pharmaceutical
biotechnology
medical device

Seniority

Senior

Perks

Retirement plan
Performance bonus
Wellness program
Paid training

Languages

English
French

Fields of study

Science
Health-related field

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Work requirements

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