CRA II

Pharmaceutical Research Associates, Inc; France; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

Une entreprise leader dans la recherche clinique recherche un Clinical Research Associate pour un rôle basé à Paris, entièrement à distance. Vous serez responsable de la gestion des sites d'investigation, en veillant à ce que les métriques cliniques clés soient atteintes. Le candidat idéal aura au moins un an d'expérience en surveillance indépendante, avec un intérêt pour l'oncologie et l'hématologie.

Qualifications

• Expérience stable en tant que CRA (minimum 1 an).
• 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 d'investigation.

Connaissances

Organisation

Communication

Multitâche

Compétences informatiques

Description du poste

Overview

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 1years of independent monitoring experience is essential

Responsibilities

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

Qualifications

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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