Backend & Flutter Engineer for Clinical Trials Platform

Centre for Human Drug Research

Netherlands

Remote

EUR 53,000 - 72,000

Full time

14 days+
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Benefits offered by this job

ABP pension
Holiday allowance 8%
Year-end bonus 3.8–12%
25 vacation days + Diversity Day
Training funding
Public transport reimbursement or bike

Job summary

Centre for Human Drug Research (CHDR) in Leiden, the Netherlands, is seeking an experienced Software Engineer to help enhance Promasys, a core data platform for clinical trial management. You will design, build, and maintain backend services and Flutter-based applications that enable accurate and efficient clinical research, working closely with researchers and other stakeholders.

The role offers a one-year contract for a minimum of 32 hours per week, with the prospect of a permanent contract.

Qualifications

  • Experience with Flutter and Dart (preferred).
  • Experience in server-side development using Java and Hibernate.
  • Understanding of object-oriented and functional programming concepts.
  • Solid knowledge of relational databases.
  • Experience publishing applications to Apple App Store and Google Play Store.
  • Familiarity with Git, Azure DevOps, and CI/CD pipelines.
  • OpenEdgeABL is a plus.

Responsibilities

  • Design, build, and maintain backend services and Flutter-based applications for Promasys.
  • Translate user needs into robust, scalable software solutions in collaboration with researchers.
  • Contribute to long-term platform stability and quality through proactive improvements.

Skills

Flutter and Dart
Java
Hibernate
OO/FP concepts
Relational databases
App Store/Play publishing
OpenEdgeABL (plus)

Tools

Git
Azure DevOps
CI/CD pipelines

Job description

Centre for Human Drug Research (CHDR) in Leiden, the Netherlands, is seeking an experienced Software Engineer to help enhance Promasys, a core data platform for clinical trial management. You will design, build, and maintain backend services and Flutter-based applications that enable accurate and efficient clinical research, working closely with researchers and other stakeholders.

The role offers a one-year contract for a minimum of 32 hours per week, with the prospect of a permanent contract.

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