Data Manager

🕒 September 3

🌐 Netherlands, Germany – Remote

🇳🇱 Netherlands – Remote 🇩🇪 Germany – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

📊 Data Scientist

👻 Ghost score 15%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Eurofins

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1987

🍽️ Food & Beverage

🏥 Healthcare

📦 Logistics

💰 $30M Grant on 2021-10

Food & Beverage • Healthcare • Logistics

Eurofins is a global leader in testing and laboratory services. With approximately 62,000 employees and over 900 laboratories across 62 countries, the company provides a wide range of testing services across various industries. Eurofins offers services such as food and feed testing, consumer product testing, genomic services, clinical diagnostics, forensic services, environment testing, and pharmaceutical testing. The company is committed to scientific innovation and sustainability, and it plays a critical role in testing for health, safety, and environmental impacts worldwide.

📋 Description

• Create Case Report Forms (eCRF/pCRF) • Develop and maintain study databases • Coordinate data entry, data cleaning, and query management • Stay familiar with current scientific developments within the task area • Participate in and organize meetings, telephone conferences, training sessions, and seminars with in-house teams and clients • Develop and implement strategies for introducing clinical research databases according to ICH, GCP, and CDISC standards • Develop (e)CRF standard modules • Create and revise data management SOPs and associated workflows • Manage projects within data management activities • Prepare study-specific schedules and timelines 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, edit checks, and data transfer • Conduct data review, data cleaning, and query management • Handle third-party and device data • Code diseases, adverse events, and drugs using study-specific systems such as WHO Drug Global or MedDRA • Organize and execute third-party and SAE reconciliation

🎯 Requirements

• 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)

🏖️ Benefits

• Full-time employment