Data Manager VITRO

Posted 9 Days Ago
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Saclay, Essonne, Île-de-France, FRA
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Manage and validate in vitro data within the VITRO application. Responsibilities include gathering requirements, functional and technical testing, database quality control, master data imports, data integrity rules, system integrations, documentation, and stakeholder collaboration. The role requires fluent French and English, a relevant master’s degree, and at least five years of data management experience, preferably in preclinical research.
Summary Generated by Built In

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. 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.

Activities

  • Collect and challenge business requirements; document meeting outcomes and key decisions.
  • Perform functional and technical testing of the VITRO application
  • Conduct data quality control on the VITRO database
  • Write and update user documentation (guides, training materials, business rules) in both French and English
  • Review and track master data imports in DEV, UAT, and PROD environments
  • Ensure functional understanding of in vitro data applications and their integration with the VITRO product
  • Validate and monitor links between VITRO and master data/reference systems
  • Implement data integrity rules and ensure compliance
  • Execute data management decisions and directives defined by the internal data manager
  • Collaborate closely with Agile team members and business 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: Minimum 5 years in data management or related fields, preferably in preclinical research
  • Skills: Strong analytical, communication, and organizational skills; autonomy and team collaboration required
  • Education: Master’s degree in a relevant scientific or technical field
  • Languages: Fluent in French and English (written and spoken)

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.

Skills Required

  • Minimum 5 years of experience in data management or related fields, preferably in preclinical research
  • Master’s degree in a relevant scientific or technical field
  • Fluent French and English, written and spoken
  • Strong analytical, communication, and organizational skills
  • Ability to work autonomously and collaboratively in a team
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The Company
HQ: Boulogne-Billancourt
697 Employees
Year Founded: 2014

What We Do

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of Full-service CRO, FSP, and Resourcing solutions guided by compassion, care, and excellence. Founded in 2014 and headquartered in Paris, France, and operating in 28 countries across Europe, USA and India, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas, with speciality focus on Oncology & Hematology, Rare Disease & Pediatrics, Infectious Disease, Inflammation & Immunotherapy, Pain Treatment & CNS, and Late Phase & RWE.

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