Clinical Trial Associate 2

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 Senior Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks.

What You Will Do:

You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges.

Key responsibilities include:

• Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.
• Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
• Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study.
• Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials.
• Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success.

Your Profile:

You will have a strong foundation in clinical trial management, 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
• Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.
• Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively.
• Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management.
• Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders.
• Willingness to travel as required (approximately 10%)

En tant qu’Associé(e) Principal(e) aux Essais Cliniques (Senior Clinical Trial Associate) chez ICON Plc

En tant que Senior Clinical Trial Associate (CTA Senior) chez ICON Plc, vous jouerez un rôle clé dans le soutien à la gestion et à l’exécution des essais cliniques en assurant diverses activités administratives et opérationnelles essentielles au bon déroulement des études.

Vos responsabilités

Vous assumerez la responsabilité de plusieurs livrables liés à la gestion des essais cliniques, en mettant à profit votre expertise pour relever des défis complexes et contribuer au succès des projets.

Principales responsabilités :

• Fournir un soutien administratif aux essais cliniques, notamment en gérant la documentation, en coordonnant les réunions et en maintenant à jour les dossiers liés aux études.
• Participer à la préparation et à la soumission des documents réglementaires, tout en veillant au respect des protocoles d’étude et des exigences réglementaires applicables.
• Collaborer avec les équipes multidisciplinaires afin de soutenir les opérations des essais cliniques et de résoudre les problèmes pouvant survenir au cours des études.
• Assurer le suivi de l’avancement des essais, notamment en gérant les communications avec les sites investigateurs et en veillant à la livraison des matériels d’étude dans les délais requis.
• Développer et maintenir des relations de travail solides avec le personnel des sites et les autres parties prenantes afin de favoriser le bon déroulement des opérations et la réussite globale des projets.

Votre profil

Vous possédez une solide expérience en soutien à la gestion des essais cliniques et êtes capable de travailler de façon autonome tout en accompagnant et en guidant vos collègues lorsque nécessaire.

Qualifications et expérience requises :

• Diplôme universitaire (Licence/Bachelor ou équivalent) dans une discipline scientifique pertinente ou un domaine lié à la santé.
• Expérience significative dans un rôle de soutien aux essais cliniques, avec une excellente compréhension des processus de recherche clinique et des exigences réglementaires.
• Excellentes compétences organisationnelles et de gestion des priorités, avec la capacité de gérer efficacement plusieurs tâches et projets simultanément.
• Maîtrise des systèmes de gestion des essais cliniques (CTMS) et des logiciels pertinents, avec une grande rigueur dans la gestion documentaire et des données.
• Excellentes compétences en communication, en relations interpersonnelles et en résolution de problèmes, avec une capacité démontrée à collaborer efficacement avec des équipes et des intervenants variés.
• Disponibilité pour des déplacements professionnels occasionnels (environ 10 % du temps ).

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