Global Clinical Trial Associate - Sponsor Dedicated, Canada Remote
- Montreal, Burlington
- Clinical Operations
- ICON Strategic Solutions
- Remote
Senior Talent Acquisition Business Partner
- Icon Strategic Solutions
About the role
Clinical Trial Associate, Remote, Canada
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Clinical Trial Associate to join our diverse and dynamic team. As a Clinical Trial Associate at ICON, you will play a pivotal role in supporting the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
What you will be doing
- Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
- Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation.
- Collaborate with cross-functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials.
- Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures.
- Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports.
Your profile
- Bachelor's or advanced degree in Life Sciences, Health Sciences, or a related field.
- Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
- Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively.
- Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance.
- Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites.
Nous recherchons actuellement un(e) Assistant(e) d’Essais Cliniques (Clinical Trial Associate) pour rejoindre notre équipe diversifiée et dynamique. En tant qu’Assistant(e) d’Essais Cliniques chez ICON, vous jouerez un rôle essentiel dans le soutien à la conception, à la mise en œuvre et à la gestion des essais cliniques, contribuant ainsi à l’avancement de traitements et thérapies innovants.
Vos responsabilités
- Assister à la planification, à l’exécution et au suivi des essais cliniques, en veillant au respect des exigences des protocoles, des directives réglementaires et des normes de l’industrie.
- Coordonner les activités de l’étude, notamment l’initiation des sites, le recrutement des patients, la collecte des données et les visites de monitoring, afin de garantir une collecte d’informations précise et dans les délais.
- Collaborer avec des équipes interfonctionnelles telles que les Opérations Cliniques, la Gestion des Données et la Biométrie pour soutenir la bonne exécution des essais.
- Maintenir une documentation d’étude complète et à jour, en veillant au respect des réglementations applicables et des procédures opératoires standard.
- Participer aux activités de clôture d’étude, y compris le nettoyage des données, l’analyse et la préparation des rapports cliniques.
Votre profil
- Licence ou diplôme avancé en sciences de la vie, sciences de la santé ou domaine connexe.
- Expérience préalable en recherche clinique ou dans le domaine de la santé, idéalement au sein de l’industrie pharmaceutique, biotechnologique ou d’une CRO.
- Excellentes compétences organisationnelles et de gestion du temps, avec la capacité de prioriser efficacement et de gérer plusieurs tâches simultanément.
- Grande attention aux détails et solides capacités de résolution de problèmes, avec un engagement envers l’exactitude, l’intégrité et la conformité des données.
- Bonnes compétences en communication et en relations interpersonnelles, avec la capacité de collaborer efficacement avec des équipes transverses et de développer de solides relations avec les équipes d’étude et les centres cliniques.
Si vous souhaitez une version plus concise, plus formelle ou adaptée à un style particulier d’offre d’emploi, je peux aussi vous en préparer une !
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
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
09/16/2025
Summary
Growing with ICON: Christina’s Journey in Clinical Operations and Quality Leadership At ICON, we are proud to showcase the incredible journeys of our colleagues who make a real impact on patients’ l
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Inside ICONContent type
BlogsPublish date
01/17/2025
Summary
Five Reasons Why You Should Work at a Contract Research Organization Contract research organisations (CROs) play a pivotal role in advancing medical science, offering career opportunities tha
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Our PeopleContent type
BlogsPublish date
11/13/2024
Summary
How to Become a Clinical Research Associate: A Step-by-Step Guide The clinical research industry is projected to reach $52.0 billion by 2026, growing at an impressive rate of 5.6% annually.
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