Data Manager VITRO

Excelya

France

Hybride

EUR 60 000 - 90 000

Plein temps

14 jours+
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Résumé du poste

Excelya is inviting you to join a dynamic, ambitious team driving innovation in the clinical research space. You will play a critical part in data management, ensuring data quality and regulatory compliance across DEV, UAT, and PROD environments.

Fluent in French and English, you’ll document requirements, perform testing, and collaborate closely with agile stakeholders to implement data integrity rules and support the VITRO product.

Qualifications

  • Minimum 5 years in data management or related fields, preferably in preclinical research.
  • Strong analytical, communication, and organizational skills; autonomy and team collaboration required.
  • Fluent in French and English (written and spoken).

Responsabilités

  • 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

Connaissances

Analytical skills
Communication skills
Organizational skills
Autonomy
Team collaboration

Formation

Master’s degree in a relevant scientific or technical field

Description du poste

JoinExcelya,whereAudacity,Care,andEnergydefinewhoweareandhowwework.Webelieveincreatingboldsolutionsandfosteringaninclusiveenvironmentwherecollaborationandindividualgrowthgohandinhand.

Thisroleisanexcitingopportunitytocontributetoadynamic,ambitiousteam.Youwillplayacriticalpartindrivinginnovation andmakinganimpactintheclinicalresearchspace,whileenjoyingastimulatingprofessionalenvironmentthatencouragespersonalandintellectualgrowth.

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
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)
WhyJoinUs?

AtExcelya,wecombinepassionforsciencewithenthusiasmforteamworktoredefineexcellenceinhealthcare.

Here’swhatmakesusunique:

Weareayoung,ambitioushealthcompanyrepresenting900Excelyates,driventobecomeEurope'sleadingmid-sizeCROwiththebestemployeeexperience.Ourone-stopproviderservicemodel—offeringfull-service,functionalserviceprovider,andconsulting—enablesyoutoevolvethroughdiverseprojects.Workingalongsidepreeminentexperts,youwillhelpimprovescientific,operational,andhumanknowledgetoenhancethepatient'sjourney.

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