Data Manager Clinique

Excelya; Boulogne-Billancourt; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

Une entreprise dynamique recherche un professionnel en gestion des données cliniques pour rejoindre une équipe ambitieuse. Le candidat idéal a une expérience en coordination d'essais cliniques, en oncologie et une solide connaissance des outils GCP. Excelya offre un environnement de travail stimulant favorisant la croissance personnelle et intellectuelle.

Qualifications

• Expérience solide en coordination d'essais cliniques et gestion de sites, notamment en oncologie.
• Maîtrise des directives GCP et ICH avec expérience en documentation d'études.
• Fluent en anglais (C1/C2); la connaissance d'autres langues est un plus.

Responsabilités

• Analyser les besoins des équipes de recherche et proposer des structures appropriées.
• Configurer REDCap, y compris la création de CRFs et la gestion des droits d'accès.
• Former les utilisateurs sur REDCap et fournir une documentation.

Connaissances

Connaissance des directives GCP

Gestion des documents d'études

Établir des relations productives

Formation

Diplôme en sciences de la vie ou médecine

Outils

REDCap

SAS

R

SQL

Description du poste

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Data Management. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main responsibilities :

• Analyzing the needs of research teams and proposing appropriate project structures within REDCap
• Full configuration of REDCap : creation of CRFs (Case Report Forms), conditional logic, access rights management, randomization setup
• Providing recommendations on best practices for clinical data collection and management
• Ensuring coherent modeling and structuring of databases to meet scientific and regulatory requirements
• Using clinical data tools such as SAS, R, and SQL for data processing, analysis, and verification
• Supporting and training users on REDCap : delivering training sessions, producing documentation, and offering ad hoc assistance

Requirements

• Experience : Solid background in clinical trial coordination and site management for global registrational studies, with mandatory oncology experience. Prior field monitoring experience (CRO or pharma) highly valued. Familiarity with CRO oversight and global clinical operations is a plus.
• Skills : Strong knowledge of GCP and ICH guidelines. Experienced in study documentation from set-up to close-out. Able to build productive relationships with external partners and internal stakeholders.
• Education : Degree in life sciences, medicine, or other relevant field.
• Languages : Full professional fluency in English (C1 / C2); additional languages are a plus.

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here’s what makes us unique

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience . Our one-stop provider service model —offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.

Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.