Data Manager Redcap

Excelya; Paris; Sur place; EUR 45 000 - 55 000; Plein temps

Résumé du poste

A growing clinical research organization in Paris is looking for a Safety team member. You will manage data management tools, especially REDCap, and design and validate Case Report Forms. Ideal candidates will have a degree in a relevant field, strong CRF design knowledge, and fluency in French and English. Join us to contribute to impactful clinical research in a collaborative environment.

Qualifications

• Proven ability to thrive in collaborative, fast-moving environments.
• Hands-on experience with REDCap is essential.
• Strong knowledge of CRF design and data validation processes.
• Degree in a relevant field.

Responsabilités

• Manage and operate data management tools, focusing on REDCap.
• Design and validate Case Report Forms (CRFs) within REDCap.
• Oversee clinical study data tracking and ensure high-quality data.
• Create and manage database freezes and coordinate data activities.
• Maintain study documentation and ensure compliance with standards.
• Prepare regular data management status reports for stakeholders.

Connaissances

Proven ability to thrive in collaborative environments

Hands-on experience with REDCap

Knowledge of CRF design

Data validation processes

Fluency in French

Fluency in English

Formation

Degree in Life Sciences, Health Sciences, Biostatistics, Bioinformatics

Outils

REDCap

Clean Web

Description du poste

About 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 offers an exciting opportunity to contribute to a dynamic, ambitious Safety team. You will play a critical role in driving innovation and making an impact in the clinical research space, within a stimulating professional environment that encourages personal and intellectual growth.

• Manage and operate data management tools, with a strong focus on REDCap (essential) and Clean Web.
• Design and validate Case Report Forms (CRFs) within REDCap.
• Oversee clinical study data tracking and ensure high-quality data collection and validation.
• Create and manage database freezes (cofreeze) and coordinate study-specific data activities.
• Maintain study documentation and ensure compliance with data management standards.
• Prepare regular data management status reports for stakeholders.

Requirements

About You

At Excelya, taking audacious steps is encouraged, so we’re looking for individuals who are ready to grow with us and share our values.

• Experience: Proven ability to thrive in collaborative, fast-moving environments. We prioritize talent over minimum years of experience!
• Skills: Hands-on experience with REDCap is essential, along with strong knowledge of CRF design and data validation processes.
• Education: Degree in Life Sciences, Health Sciences, Biostatistics, Bioinformatics, or related fields.
• Languages: Fluency in French & English.

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 with 900 Excelyates, aiming to become Europe’s leading mid-size CRO with the best employee experience. Our comprehensive service model offers full-service, functional service provider, and consulting options, enabling you to work on diverse projects. Collaborate with preeminent experts to improve scientific, operational, and human knowledge, enhancing the patient journey.

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