Eurofins

Global lab testing and analytics network

Data Manager

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeHamburg, GermanyNo salary listedRemote

About the Job

Requirements

A university degree in natural sciences or another comparable field is required.
Working knowledge of International Council for Harmonisation Good Clinical Practice guidelines is required.
Fluency in written and spoken English is required.

Responsibilities

Become familiar with current scientific developments within the scope of the task area.
Participate in and organize in-house and client meetings, telephone conferences, training sessions, and seminars.
Develop and implement strategies for introducing clinical research databases in accordance with applicable International Council for Harmonisation Good Clinical Practice and Clinical Data Interchange Standards Consortium standards.
Develop electronic and paper Case Report Form standard modules.
Create and revise data management standard operating procedures and their associated workflows.
Manage projects within the scope of data management activities.
Prepare study-specific schedules and timelines for tasks related to the function in coordination with relevant departments.
Create and adhere to audit-specific Data Management Plans and related documents.
Define, program, and validate completeness and plausibility checks, including edit checks and data transfer.
Review and clean data and manage queries.
Handle third-party data and device data.
Code diseases, adverse events, and drugs according to study-specific coding systems such as World Health Organization Drug Global and Medical Dictionary for Regulatory Activities.
Organize and execute third-party and serious adverse event reconciliation.

Desired Qualifications

Experience developing data structures according to Clinical Data Interchange Standards Consortium standards is desirable.

Job 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.

Qualifications

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)

Additional Information

Contacts by headhunters, recruiting or staffing agencies are not accepted!

Please send your application including anticipated salary.

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size: 10,001+
Company stage: IPO
Headquarters: Luxembourg
Founded: 1987

Recently Posted Jobs

Explore more opportunities at Eurofins

See more jobs