Clinical Database Programmer

A
AlimentivClinical trials
Listing location: Dublin / Cambridge / London / Lisboa / Bucharest / Budapest / Warsaw / Krakow / Ljubljana / Sofia; Workplace type: RemoteFull-Time
Salary not disclosed
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Job Details

Required Skills
C#

Requirements

  • Have a degree or diploma in Computer Science, Information Technology, or a related field, or equivalent relevant experience.
  • Have previous experience in clinical database development, EDC programming, or clinical study builds.
  • Have previous experience within a CRO or pharmaceutical environment.
  • Know eCRFs, edit checks, database testing, and clinical data management processes.
  • Understand programming principles, logic, and database development.
  • Have experience supporting EDC integrations, technical initiatives, or bid defence activities.
  • Bring analytical, problem-solving, and organisational skills.
  • Have hands-on Medidata Rave experience, including study builds and configuration (nice to have).
  • Have knowledge of C# programming and developing custom functions within Medidata Rave (nice to have).
  • Have experience with AI tools, automation, or AI-assisted programming (nice to have).

Responsibilities

  • Design, build, test, and maintain clinical study databases within EDC systems.
  • Develop and configure eCRFs, edit checks, and study-specific database requirements.
  • Support clinical data transfers, integrations, and database validation activities.
  • Troubleshoot technical issues and provide ongoing EDC study support.
  • Collaborate with Data Management, project teams, and sponsors to support study delivery.
  • Contribute to process improvements, automation, and AI-related initiatives.
  • Support multiple clinical studies and progressively take ownership of study builds.
  • Maintain database documentation, quality standards, and study timelines.
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