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# Data Manager

- **Company:** Eurofins Bioskin
- **Location:** Hamburg, Germany
- **Contract:** Permanent contract
- **Skills:** Databases, Data Cleansing, Data Transmissions, Data Structures, Data Processing, Data Management
- **Published:** September 6, 2026
- **Apply:** https://www.careerjet.de/jobad/debc1cbdbcfb58ee8f2ba763d6603af692

## About the Role

* University degree in natural sciences or other comparable degree
 * Working knowledge of ICH GCP guidelines
 * Experience in development of data structures according to CDISC standards would be a nice to have
 * Dependable, well-structured and organized, target-oriented personality, team player
 * Well versed in English (written and spoken)

## Description

We are looking for an Data Manager in clinical trials to join our team at Eurofins bioskin. The Data Manager is responsible for creating Case Report Forms (eCRF/pCRF), developing and maintaining study databases, and coordinating data entry, data cleaning, and query management.
Your main responsibilities:

 * Familiarization with current scientific developments within the scope of the task area
 * Participation in/organization of meetings and telephone conferences in-house / with clients / training sessions, seminars
 * Development and implementation of strategies for the introduction of clinical research databases in accordance with the applicable international standards (ICH, GCP, CDISC) and
 * Development of (e)CRF standard modules and
 * Creation and revision of data management SOPs and the workflows described therein
 * Project management within the scope of DM activities
 * Preparation of a study-specific schedule/schedule (timelines) of tasks related to the function in coordination with the relevant departments
 * Creation and adherence to the audit-specific Data Management Plan and related documents
 * Definition, programming and validation of completeness and plausibility checks (edit checks) and data transfer.
 * Data review, data cleaning and query Management
 * Third Party data / Device data handling
 * Coding of diseases, adverse events and drugs according to study-specific coding systems, e.g. WHO Drug Global or MedDRA.
 * Organization and execution of third party and SAE reconciliation.


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