Data Manager Clinique
Excelya
il y a 2 jours
Date de publicationil y a 2 jours
S/O
Niveau d'expérienceS/O
Temps pleinType de contrat
Temps pleinDonnées / Big dataCatégorie d'emploi
Données / Big dataAbout the Job
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.
Benefits
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.
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.
Benefits
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.
RÉSUMÉ DE L' OFFRE
Data Manager Clinique
Excelya
Boulogne-Billancourt
il y a 2 jours
S/O
Temps plein
Data Manager Clinique