2

Remote Clinical Research Jobs in Quebec (NOW HIRING)

Study Start Up Associate I - Montreal, Canada-Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

... clinical testing and are used in hospitals, reference laboratories, research facilities , and ... Additional information about remote work will be provided by the interview team. Discover the ...

TailorCare is a remote-first company with our corporate office located in Nashville. This is a ... Drive cross-functional partnership with Medical Economics, Clinical Operations, Product, and the ...

Apollo Applied Research is a virtual medical clinic offering its patients an accessible path to ... The Opportunity Apollo has clinical hours available for a psychiatrist to primarily support our ...

Remote Clinical Research information

See Quebec salary details

$13

$50

$103

How much do remote clinical research jobs pay per hour?

As of Jul 30, 2026, the average hourly pay for remote clinical research in Quebec is $50.98, according to ZipRecruiter salary data. Most workers in this role earn between $30.77 and $61.06 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Remote Clinical Research position, and why are they important?

To thrive in Remote Clinical Research, a strong background in life sciences, research methodologies, and clinical trial protocols is essential, often supported by a relevant bachelor’s or master’s degree. Familiarity with tools such as Electronic Data Capture (EDC) systems, CTMS (Clinical Trial Management Systems), and certifications like Good Clinical Practice (GCP) are highly valued. Exceptional written and verbal communication, self-motivation, and organizational skills help remote researchers successfully collaborate and manage studies from a distance. These skills ensure rigorous data integrity, compliance with regulations, and effective teamwork in a remote setting.

What is a Remote Clinical Research job?

A Remote Clinical Research job involves conducting and managing clinical trials and research studies from a remote location, rather than in a traditional on-site setting. Responsibilities may include data collection, regulatory compliance, patient monitoring, and communication with study teams. These roles often use digital tools and electronic data capture systems to ensure research integrity and efficiency. Remote clinical research professionals typically work for pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. This job offers flexibility while still contributing to medical advancements and patient care.

What are some unique challenges and benefits of working in a remote clinical research role?

Working remotely in clinical research often requires you to be highly independent, organized, and proficient with digital collaboration tools, as you'll be coordinating with cross-functional teams and managing regulatory documentation from a distance. One challenge can be maintaining consistent communication with clinical sites and colleagues across different time zones, but many companies provide robust digital platforms to facilitate this. On the plus side, remote roles offer flexibility and a better work-life balance while still allowing you to contribute to impactful research. Many remote clinical research professionals report developing strong self-discipline and process management skills, which can open doors to advanced positions such as Clinical Research Associate or Project Manager.

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 Remote Clinical Research jobs in Quebec? For Remote Clinical Research jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Research jobs in Quebec look for? The top searched job categories for Remote Clinical Research jobs in Quebec are:
Infographic showing various Remote Clinical Research job openings in Quebec as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $106,038 per year, or $51 per hour.

Senior Clinical Research Associate

Icon plc

Montreal, QC • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 11 days 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