Clinical Research Associate II

PSI CRO; Saint-Maur-des-Fossés; Hybride; EUR 35 000 - 50 000; Plein temps

Résumé du poste

PSI CRO, une organisation de recherche clinique de premier plan, recherche un Clinical Research Associate pour rejoindre son équipe en France. Le rôle implique une variété de tâches de suivi dans diverses indications thérapeutiques tout en maintenant les normes de qualité les plus élevées. Vous aurez l'opportunité de vous développer professionnellement et d'acquérir une expertise précieuse dans le domaine.

Prestations

Opportunité de développement professionnel

Horaires de travail flexibles

Option de travail à domicile

Formation approfondie

Culture d'entreprise développée

Jours de congé supplémentaires (12 jours de RTT)

Qualifications

• Expérience de monitoring indépdente sur site en France.
• Expérience en suivi de visites de Phase II et/ou III.
• Maîtrise de l'anglais en pleine capacité de travail.

Responsabilités

• Conduire et rapporter tous types de visites de monitoring sur site.
• Gérer la communication et la gestion des sites.
• Participer à la recherche de faisabilité.

Connaissances

Communication

Collaboration

Résolution de problèmes

Planification

Multitâche

Formation

Diplôme Collège/Université en Sciences de la Vie

Outils

MS Office

Description du poste

Company Description

PSI is a leading Contract Research Organization with more than 22 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Independent on-site monitoring experience in France
• Experience in all types of monitoring visits in Phase II and/or III
• Experience in oncology, hemophilia, infectious diseases, GI
• Full working proficiency in English
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel

Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

We offer:

• Big professional advancement opportunity within Clinical Operations with specific mentorship and training program
• Development opportunities acrossPSI departments
• Flexible working hours
• Home-office option available, as well as combination of home and office work arrangement
• Extensive onboarding trainings and professional development training programs
• Highly developed company culture and positive team atmosphere
• Additional leave days (12 days of RTT)