Apply now

Posted 26 days ago

Senior Clinical Research Associate

@ ICR Canada - CAN

Burlington, ON · British Columbia · Alberta · Montréal, QC

On-siteFull-time3+ years experienceBilingual
Apply now
SIGNALS

Overview

ICON Canada is hiring a Senior Clinical Research Associate to monitor clinical studies at investigative sites or remotely, ensuring trials follow the protocol, SOPs, ICH-GCP and regulatory requirements. The role requires at least 3 years of clinical monitoring experience, bilingual English/French, and up to 70% travel. The posted salary range is $108,576 to $135,720 per year.

Responsibilities:

  • Surveiller les progrès des études cliniques sur les sites ou à distance
  • Vérifier la conformité au protocole, aux SOPs et à l'ICH-GCP
  • Assurer la documentation et le signalement des études
  • Respecter les exigences réglementaires applicables

Requirements summary:

  • Baccalauréat scientifique ou en santé, ou équivalent
  • Au moins 3 ans d'expérience en surveillance clinique (niveau 3)
  • Connaissance de l'ICH et des règlements sur les essais de médicaments
  • Bilingue anglais et français requis
  • Expérience en oncologie préférable
  • Capacité de voyager à 70 %

Tools & skills

Benefits mentioned

Health insuranceDentalVisionDisability insuranceRetirement planEmployee assistance
Source and dates

Employer career site / ATS feed · workday

Employer posting date
2026-10-11
First seen by our source
2026-10-12
Source record updated
2026-11-05

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SenioritySenior
DepartmentAllied health
Experience3+ years
Hours per week40 (estimated)
Travelair: moderate · ground: moderate
Work settingHome, Client sites
PositionSitting and standing
Physical demandsphysical low · computer high
LanguagesEnglish, French
EducationBachelor’s degree (required)
Fields of studyScience, Health-related field
Perks mentionedRetirement plan, Performance bonus, Wellness, Paid training

Summary and details written by AI from the posting; the employer’s posting is the authority.

ICR Canada - CAN

FieldValue
Open jobs on Jobsy14
Job description
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.


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:

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

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

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 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.

#LI-REMOTE

#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

Similar jobs

  • Clinical Research Associate II (GTA)

    Oakville, ON
    $81k–$131k/yrRemoteFull Time

    AbbVie

    2+ YOECandidates need at least 2 years of clinically related monitoring experience, including on-site monitoring of investigational drug or device trials. They also need in-depth knowledge of GCP, ICH guidelines and clinical research regulations, plus strong organization and communication skills.

    Microsoft Outlook, Microsoft PowerPoint, Microsoft Excel, Microsoft Word

    Clinical Research Associate II

    Toronto, ON
    $81k–$131k/yrRemoteFull Time

    AbbVie

    2+ YOECandidates need at least 2 years of clinical monitoring experience, including on-site monitoring of investigational drug or device trials. They need in-depth knowledge of clinical research regulations and ICH/GCP guidelines, strong organizational and communication skills, and comfort with Microsoft Office and technology.

    Microsoft Outlook, Microsoft PowerPoint, Microsoft Excel, Microsoft Word

  • Sr. Clinical Research Associate

    Mississauga, ON
    $86k–$136k/yr

    Novo Nordisk

    5+ YOECandidates need a bachelor's degree in life sciences or a related field and 5+ years of CRA experience. They must know ICH-GCP, use clinical trial systems such as EDC, CTMS and eTMF, and be able to travel up to 70% of the time.

    EDC, CTMS, eTMF

  • Senior Clinical Research Associate

    Burlington, ON
    RemoteFull Time

    ICR Canada - CAN

    Candidates need a bachelor's degree in a scientific or healthcare field and extensive CRA experience, including current oncology monitoring. They must manage several sites at once, know clinical trial software, and communicate well with stakeholders.

    Clinical trial software

    Senior Clinical Research Associate

    Burlington, ON +3
    On-siteFull Time

    ICR Canada - CAN

    1+ YOECandidates need a bachelor's degree or equivalent in a scientific or health field, or a licensed health professional background such as a registered nurse. They need 1+ years of clinical monitoring experience for level 2, or 3+ years for level 3, plus bilingual English and French.

    Clinical research, Clinical trials, Google Cloud, Bilingualism, English, French

    Senior Clinical Research Associate

    Montréal, QC +1
    On-siteFull Time

    ICR Canada - CAN

    3+ YOEICON Canada needs a bachelor's degree or equivalent, 3+ years of clinical monitoring experience for level 3, and knowledge of ICH and regulatory rules for drug trials. Bilingual English and French is required, and 70% travel is expected.

    Clinical research, Clinical trials, Google Cloud, Bilingualism, English, French

  • Senior Clinical Research Associate

    Toronto, ON
    $120k–$150k/yrRemoteFull Time

    PSI CRO

    Candidates need a college or university degree in life sciences or equivalent experience, plus independent onsite monitoring experience in Phase II and/or III trials. Full English proficiency, MS Office skills, travel ability and a valid driver's licence are required.

    MS Office

  • Clinical Research Associate

    Ottawa, ON
    $80k–$85k/yrContract, Temporary

    adecco

    2+ YOECandidates need at least 2 years of experience conducting clinical studies and knowledge of clinical research regulations and quality standards. A science bachelor's degree is preferred, and experience with medical devices, diagnostics or Veeva TMF is an asset. Candidates must be legally eligible to work and reside in Canada.

    Veeva

Locations & environments

Locations

All of CanadaRemote · Hybrid · On-site · Field

Pro tip: add remote jobs to widen your search.

Exclude locations

Workplace type

Company jobs in these results

These are this company’s jobs loaded in your current search. The company may have more openings.