ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
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.
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
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
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