Data Coordinator - CRO (Leuven, Entry-Level)

TL;DR

Data Coordinator - CRO (Leuven, Entry-Level) (Clinical Data Management): Validating and reconciling clinical study data, maintaining study documentation, and reporting data trends with an accent on accuracy, database quality, and cross-functional collaboration. Focus on identifying data conflicts, resolving discrepancies with global research sites, and supporting reliable clinical research outcomes.

Location: Full-time, office-based role in Leuven, Belgium. Occasional work from home may be available for eligible positions after training.

Company

Full-service clinical contract research organization providing clinical development services to biotechnology, pharmaceutical, and medical device companies across more than 40 countries.

What you will do

• Participate in clinical data management projects as part of a collaborative team.
• Validate clinical study database designs and reconcile data from multiple sources.
• Identify data conflicts, quality issues, metrics, and data trends.
• Collaborate with global research sites to resolve data discrepancies.
• Create and maintain study documentation.

Requirements

• Bachelor’s degree in Life Sciences or Mathematics.
• Strong attention to detail and accuracy.
• Excellent working knowledge of Microsoft Excel and Word.
• Solid oral and written English communication skills required.

Culture & Benefits

• Extensive onboarding and training program with on-site mentors.
• Defined career paths and ongoing professional development opportunities.
• Collaborative environment focused on scientific excellence, continuous learning, and cross-functional work.
• Health, wellness, retirement, and paid time off benefits, varying by country.
• Competitive compensation and company-sponsored social events.

Hiring process

• Application review by the hiring team.
• Selected candidates are contacted for an interview.