Clinical Research Associate

Pharmaceutical Research Associates, Inc; Paris; Hybride; EUR 40 000 - 70 000; Plein temps

Résumé du poste

Une entreprise innovante recherche un Clinical Research Associate passionné pour rejoindre une équipe dédiée à un client pharmaceutique mondial. Ce rôle vous permettra de gérer des sites d'investigation, d'assurer l'intégrité des données cliniques et de développer des relations solides avec le personnel des sites. Vous aurez l'opportunité de travailler dans un environnement dynamique et stimulant, contribuant à l'avancement des essais cliniques dans des domaines thérapeutiques variés. Si vous êtes motivé, fiable et prêt à relever des défis, cette opportunité est faite pour vous.

Qualifications

• Expérience de 2-3 ans en tant que CRA dans l'industrie pharmaceutique ou CRO.
• Compétences organisationnelles et 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 selon le plan de surveillance clinique.
• Développement de relations efficaces avec le personnel des sites d'investigation.

Connaissances

Gestion de projet

Compétences en communication

Compétences organisationnelles

Compétences informatiques

Capacité à travailler sous pression

Multitâche

Bilingue français-anglais

Formation

Diplôme en sciences de la vie

Description du poste

Overview

We are constantly looking for motivated, reliable and dedicated CRAs who can demonstrate at least 12 months independent external monitoring of commercial studies (or a mix of commercial clinical studies) ideally in Oncology and Hematology. Other therapeutic areas are also of interest, especially if gained on phase I - II or III commercial trials.

As a Clinical Research Associate you will be dedicated to one of our global pharmaceutical clients; with whom ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in our exclusive programs.

We are currently looking for a Clinical Research Associate to join one of our sponsor-dedicated teams in Paris (2 days ICON office based).

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 on 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, this within the pharmaceutical industry or a CRO (min 2-3 years).
• Interest in different Therapeutic Areas.
• 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.