CRA II

ICON Strategic Solutions; France; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

Une entreprise internationale de recherche clinique recherche un Clinical Research Associate basé à Paris. Vous serez responsable de la gestion des sites d'investigation et de l'assurance de l'intégrité des données cliniques. Ce poste requiert une expérience préalable en monitoring et un intérêt pour l'oncologie et l'hématologie.

Qualifications

• Minimum 1 an d'expérience en monitoring indépendant.
• Intérêt pour l'oncologie et l'hématologie.
• Capacité à travailler dans un environnement dynamique.

Responsabilités

• Gestion complète des sites d'investigation pour les études assignées.
• Planification et réalisation de visites de sites.
• Développement de relations efficaces avec le personnel des sites.

Connaissances

Organisation

Communication

Multitâche

Compétences IT

Description du poste

As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical partners - a collaboration built on shared values of innovation, flexibility, and a joint mission to bring life-changing treatments to patients faster.

This is your opportunity to be part of an exclusive, high-impact program where you can lead by example and shape the standard for clinical excellence.

• Location: Paris-based role - fully home based
• Profile: We welcome experienced CRA professionals from either CRO or pharmaceutical industry backgrounds.
• Requirement: Minimum 1 years of independent monitoring experience is essential

Key responsibilities include:

• Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out
• Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan
• Developing effective relationships with investigator site staff to ensure that key clinical metrics are met
• Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues
• Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines

You will need:

• A first stable experience as a CRA (min 1 year)
• Interested in oncology and hematology
• Excellent organization skills
• Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
• Strong IT skills
• Strong communication with the ability to multitask and work effectively under pressure
• Fluency in French and professional proficiency in English

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