Data Manager Service For biologics
7 days ago
Gi Group Consulting, a subsidiary of Gi Group Holding, is a company specializing in intellectual services within the Life Sciences sector. We dedicate our expertise to supporting our clients, including pharmaceutical groups, CROs, and biotechnology companies.
As part of our ongoing commitment to innovation, we are seeking a
Data Manager Service for Biologics (M/F)
for a consultancy mission starting in
November 2025
in
Ballerup
,
Denmark
. The role will involve contributing to the integration of scientific data generated at our client's site. The associated activities will be carried out in collaboration with multidisciplinary teams, including data managers, researchers, data governance teams, and IT product teams.
Our client is an international pharmaceutical company dedicated to biologics research and development (e.g., antibodies), aimed at creating innovative treatments for various therapeutic areas.
Description of the scientific tasks entrusted
- Collection of business needs (challenge of needs, reports, etc.),
- Testing of the technical and functional evolutions of expert software.
- File integration/Database Quality Control.
- Writing/updating of documentation related to expert software, data flows and data products (User Guide, training support, description of business rules, etc.) in English.
- Review and manage data masters imported into the DEV, UAT and PROD instances: state of play at the start of production and change tracking document.
- Functional understanding of applications managing vitro/vivo/sequencing data and their integrations into our IT ecosystem.
- Understanding links between MDMs; expert tools and the data platform: validating links, data flows and monitoring their evolution.
- Implementing Data Integrity Rules and FAIR principles.
- Help with the design and implementation of new data models.
- Implementation of the directives and decisions made by the internal data management manager.
- Collaboration with AGILE teams of data products (vitro/vivo) and business lines.
Profile
- Master's degree or higher with extensive experience in pharmaceutical research.
- Solid knowledge of preclinical research, pharmacology, toxicology, in vitro biology, and reference systems such as MDM and non-MDM.
- Proficiency in IT tools, including expertise in Excel and SQL, along with skills in functional application testing.
- A proactive mindset with strong autonomy, a results-oriented approach, and a focus on quality.
- Excellent interpersonal and organizational skills.
- Known for precision, analytical thinking, and attention to detail. Demonstrates strong teamwork abilities, effective communication skills, and ease in interacting with diverse stakeholders.
- Professional proficiency in English is essential.
Do you want to join a dynamic and ambitious Group?
Does the position align well with your expectations and skills?
Don't hesitate any longer and apply now
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