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ICON Strategic Solutions

Senior Clinical Trial Associate

Canada

Job type: Full-time
Posting language: English · French
Posted: Sep 12, 2026

Apply About employer

Applications open in a new tab.

Original job description

English section of this bilingual listing.

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Senior Clinical Trial Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency. This is a sponsor dedicated position focused on Oncology trials.

What You Will Do

You will lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement.

Key Responsibilities Include

Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines.
Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies.
Overseeing site management and monitoring to ensure data integrity and compliance with study protocols.
Providing guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards.
Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.

Your Profile

You will have a strong foundation in clinical coordination, with the experience to work independently and guide others.

Required Qualifications And Experience

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.
Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges.
Oncology experience required

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

Read the full bilingual original

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Senior Clinical Trial Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency. This is a sponsor dedicated position focused on Oncology trials.

What You Will Do

You will lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement.

Key Responsibilities Include

Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines.
Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies.
Overseeing site management and monitoring to ensure data integrity and compliance with study protocols.
Providing guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards.
Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.

Your Profile

You will have a strong foundation in clinical coordination, with the experience to work independently and guide others.

Required Qualifications And Experience

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.
Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges.
Oncology experience required

Associé(e) principal(e) aux essais cliniques (Oncologie)

Il s'agit d'une excellente opportunité pour un(e) professionnel(le) expérimenté(e) en coordination d'essais cliniques souhaitant jouer un rôle clé dans la conduite d'études en oncologie au sein d'un modèle dédié à un commanditaire chez ICON. Ce poste offre la possibilité de contribuer directement à l'exécution d'essais cliniques complexes en collaborant étroitement avec des équipes multidisciplinaires, des investigateurs et des centres afin de garantir la qualité, la conformité réglementaire et le succès des études.

Le ou la candidat(e) idéal(e) possédera une solide expérience en coordination et en gestion d'essais cliniques, une excellente connaissance des Bonnes Pratiques Cliniques (BPC/GCP) et des exigences réglementaires, ainsi qu'une expérience démontrée dans le domaine de l'oncologie. Ce rôle convient parfaitement à une personne autonome, capable de gérer plusieurs priorités simultanément, d'identifier de manière proactive les risques potentiels et de mettre en œuvre des solutions efficaces pour assurer la réussite des études.

Qualifications Requises

Diplôme universitaire (baccalauréat/licence) dans une discipline scientifique ou liée aux soins de santé.
Expérience significative en coordination ou en gestion d'essais cliniques.
Expérience en recherche clinique dans le domaine de l'oncologie (obligatoire).
Solide connaissance des BPC (ICH-GCP) et des exigences réglementaires applicables aux essais cliniques.
Expérience en soutien à la gestion et au suivi des centres investigateurs.
Excellentes compétences organisationnelles, de communication et de résolution de problèmes.
Capacité à travailler de façon autonome tout en collaborant efficacement avec diverses parties prenantes.
Grande attention aux détails et approche proactive pour assurer la réussite des études.

Pourquoi rejoindre cette opportunité ?

Ce poste vous permettra de contribuer à l'avancement de la recherche en oncologie tout en travaillant au sein d'une organisation reconnue mondialement pour son engagement envers la qualité, l'innovation et l'amélioration des résultats pour les patients. Vous aurez l'occasion d'élargir votre expertise, d'assumer des responsabilités à forte valeur ajoutée et de jouer un rôle essentiel dans le succès des essais cliniques.

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

Apply About employer

More about this job

Responsibilities

Coordinate and oversee oncology clinical trial activities, ensuring compliance with protocols and regulatory requirements, data integrity, quality, and project timelines. Collaborate with study teams, investigators, and sites, support clinical staff, track progress, and identify and mitigate risks.

Requirements

A bachelor's degree in a scientific or healthcare-related discipline and significant clinical trial coordination or management experience are required. Candidates must have oncology research experience, knowledge of ICH-GCP and applicable regulations, and strong organizational, communication, problem-solving, and collaboration skills.

Skills

Clinical Trial Coordination
Clinical Trial Management
Oncology
ICH-GCP
Regulatory Compliance
Clinical Site Management
Site Monitoring
Protocol Adherence
Data Integrity
Risk Management
Project Management
Problem-Solving
Communication
Cross-Functional Collaboration
Quality Improvement
Clinical Research

Benefits

Annual Leave
Health Insurance
Retirement Planning
Employee Assistance Programme
Life Assurance
Childcare Vouchers
Bike Purchase Schemes
Discounted Gym Memberships
Subsidized Travel Passes
Health Assessments

Visa sponsorship

Not detected in the job text

Keywords

Clinical Trials
Oncology
Clinical Trial Coordination
Clinical Trial Management
Clinical Research
ICH-GCP
Good Clinical Practice
Regulatory Requirements
Clinical Protocols
Site Management
Site Monitoring
Investigators
Data Integrity
Quality Compliance
Project Timelines
Risk Mitigation
Cross-Functional Teams
Continuous Improvement
Study Execution
Pharmaceutical Manufacturing

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