Clinical Trial Associate

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

As a Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

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:

You will bring relevant clinical coordination experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a relevant scientific discipline or healthcare-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.
Willingness to travel as required (approximately 60%)

En tant que Chargé(e) de recherche clinique chez ICON, vous participerez à la conception, à la mise en œuvre et à la gestion des essais cliniques, contribuant ainsi au développement de traitements et de thérapies innovants.

Vos missions

Vous contribuerez aux activités de coordination clinique tout en étant responsable de vos livrables et en travaillant de manière collaborative avec les équipes.

Vos principales responsabilités incluent :

Assister à la planification, à l’exécution et au suivi des essais cliniques, en veillant au respect des protocoles, des exigences réglementaires et des normes de l’industrie.
Coordonner les activités des études, notamment la mise en place des centres, le recrutement des patients, la collecte des données et les visites de suivi, afin d’assurer une collecte et une documentation des données précises et dans les délais.
Collaborer avec des équipes transverses, notamment les Opérations Cliniques, la Gestion des Données et la Biostatistique, afin de soutenir la bonne exécution des essais cliniques.
Maintenir une documentation complète et précise des études, en conformité avec les réglementations applicables et les procédures opératoires standard.
Participer aux activités de clôture des études, y compris le nettoyage des données, le support à l’analyse et la préparation des rapports d’études cliniques.

Votre profil

Vous justifiez d’une expérience pertinente en coordination clinique et possédez les compétences et qualifications suivantes.

Qualifications et expérience requises :

Licence ou diplôme universitaire dans une discipline scientifique ou dans le domaine de la santé.
Expérience préalable en recherche clinique ou dans le secteur 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 gérer efficacement des priorités concurrentes.
Fort sens du détail et bonnes capacités d’analyse et de résolution de problèmes, avec un engagement envers l’exactitude, l’intégrité et la conformité des données.
Excellentes compétences en communication et en relations interpersonnelles, avec la capacité de collaborer de manière transversale et d’établir des relations solides avec les équipes d’étude et les centres investigateurs.
Disponibilité pour des déplacements professionnels à hauteur d’environ 60 %.

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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised 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

Clinical Trial Associate

Vos missions

Votre profil

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