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 Trial Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency.

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.

En tant qu’Attaché(e) de Recherche Clinique (Clinical Trial Associate) chez ICON, vous superviserez et soutiendrez la mise en œuvre des essais cliniques, en garantissant les plus hauts standards de qualité, de conformité et d’efficacité.

Vos Missions

Vous serez en charge des activités de coordination clinique nécessitant une expertise technique, avec un fort accent sur la qualité et l’amélioration continue.

Vos Principales Responsabilités Incluent

Assurer la gestion et la coordination des activités liées aux essais cliniques afin de garantir le respect des protocoles, des exigences réglementaires et des délais des projets. Collaborer avec des équipes pluridisciplinaires pour résoudre les problématiques liées aux essais, optimiser les processus et assurer une exécution efficace des études. Superviser la gestion des sites et le suivi (monitoring) afin de garantir l’intégrité des données et la conformité aux protocoles. Fournir un accompagnement et un support aux équipes cliniques et aux investigateurs, en veillant au respect des bonnes pratiques et des normes réglementaires. Suivre et analyser l’avancement des essais, identifier les risques potentiels et mettre en œuvre des stratégies pour anticiper et atténuer les difficultés.

Votre Profil

Vous disposez de solides bases en coordination clinique, avec la capacité de travailler de manière autonome et d’accompagner d’autres collaborateurs.

Qualifications Et Expérience Requises

Diplôme de niveau licence (Bachelor) dans une discipline scientifique ou dans le domaine de la santé Expérience significative en gestion d’essais cliniques, avec une excellente connaissance des processus et des exigences réglementaires Capacité démontrée à gérer simultanément plusieurs projets, avec d’excellentes compétences organisationnelles et en résolution de problèmes Excellentes compétences en communication et en relations interpersonnelles, avec une capacité à collaborer efficacement avec des équipes et des parties prenantes variées Sens du détail et approche proactive pour assurer le succès des essais et anticiper les défis 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