Les missions du poste
Join Excelya and Make a Difference in Clinical Research In Vivo
As part of the deployment of the new VIVO solution (Benchling application), the Data Sciences & Data Management department is seeking operational support to assist with the implementation, testing, validation, and documentation of the application.
The mission will be carried out in close collaboration with multidisciplinary teams including Data Management, Business teams, Referential teams, and the VIVO Product Team.
Key Responsibilities:
- Support the implementation and validation of the Benchling / VIVO application
- Perform functional testing and data consistency checks across systems (Benchling, VIVO DB, LIMS, BI tools, FederateS)
- Validate and monitor links with referential systems (MDM and nonMDM)
- Support the Product Owner and Business Owner in prioritizing and implementing product enhancements
- Execute User Story testing in an Agile environment in line with defined test plans
- Contribute to user and functional documentation
- Understanding of in vivo study designs, preclinical pharmacology, and toxicology data requirements. Familiarity with related laboratory information management systems (LIMS) and experimental data integration is a plus.
Le profil recherché
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.
Qualifications & Skills Required
- Master degree in Life Sciences, Biology, Pharmacology, or a related field.
- Proven experience in data management for in vivo or preclinical research studies.
- Business analysis and functional testing experience (UAT experience)
- Knowledge of laboratory environments, biology, and preclinical research
- Understanding of pharmacology, toxicology, and PK
- Knowledge of referential systems (MDM and nonMDM)
- Strong proficiency in Excel and basic SQL skills
- Ability to work in an Agile / SCRUM environment
- Fluent in English and French (written and spoken)
Bienvenue chez Excelya
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 our values Energy, Care and Audacity.
Founded in 2014 and headquartered in Paris, France, 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.
We take a one-team approach to work: our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.
Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.
Publiée le 15/04/2026 - Réf : 6f7f3ce4-0a74-440f-965c-c23a24f08adf
