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At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

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

Key responsibilities include:

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:

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

Required qualifications and experience:

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required (approximately 60%)

En tant que CRA II chez ICON

En tant que CRA II (Clinical Research Associate II) chez ICON, vous participerez à la conception et à l’analyse des essais cliniques, à l’interprétation de données médicales complexes et contribuerez à l’avancement de traitements et thérapies innovants.

Vos responsabilités

Vous contribuerez aux activités de suivi des essais cliniques, en assumant la responsabilité de vos livrables et en travaillant en étroite collaboration avec les différentes parties prenantes.

Vos principales responsabilités incluront :

• Réaliser les visites de sélection, d’initiation, de suivi et de clôture des centres participant aux essais cliniques.
• Veiller au respect du protocole, à l’intégrité des données et à la sécurité des patients tout au long de l’étude.
• Collaborer avec les investigateurs et les équipes des centres afin de garantir le bon déroulement des études.
• Effectuer la revue des données et la résolution des demandes de clarification (queries) afin de maintenir un haut niveau de qualité des données cliniques.
• Contribuer à la préparation et à la révision de la documentation d’étude, notamment les protocoles et les rapports d’étude clinique.

Votre profil

Vous possédez une expérience pertinente en monitoring d’essais cliniques ainsi que les qualifications et compétences suivantes.

Qualifications et expérience requises :

• Licence/Bachelor ou diplôme équivalent dans un domaine scientifique ou lié aux soins de santé.
• Minimum de 2 ans d’expérience en tant qu’Attaché(e) de Recherche Clinique (ARC/CRA).
• Excellente connaissance des processus d’essais cliniques, de la réglementation applicable et des Bonnes Pratiques Cliniques (ICH-GCP).
• Solides compétences organisationnelles et de communication, avec un grand souci du détail.
• Capacité à travailler de manière autonome tout en collaborant efficacement dans un environnement dynamique et en constante évolution.
• Disponibilité pour des déplacements professionnels fréquents (environ 60 % du temps).

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.

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.