Remote Clinical Data Programmer & EDC Specialist

iTRTech Group; Portugal; Presencial; EUR 28 000 - 31 000; Tempo integral

Resumo da oferta

iTRTech Group is offering a fully remote role for a Clinical Data Programmer/Manager (EDC). You will manage data lifecycle activities from study start-up to database lock, combining data management, programming, and system implementation tasks across HealthTech projects.

The ideal candidate brings 3+ years in clinical trials with EDC experience, SAS programming skills, and strong collaboration with sponsors and cross-functional teams, while maintaining regulatory compliance.

Qualificações

• Bachelor’s degree or equivalent education and experience.
• Minimum of three years in clinical trials or a closely related area.
• Hands‑on experience with Electronic Data Capture (EDC) systems.
• Understanding of clinical databases, CRFs, and eCRFs.
• Experience across the clinical data lifecycle.
• Knowledge of Good Clinical Data Management Practices and related documentation.
• English proficiency at B2/C1 level.

Responsabilidades

• Configure and implement studies using eClinical/EDC platforms.
• Write specifications for forms, reports, workflows, and system components.
• Support system validation, testing, and UAT.
• Coordinate data transfers, loading, and integration tasks.
• Prepare data for delivery to sponsors and external parties.

Conhecimentos

Attention to detail

English proficiency

Organisational skills

Multitasking

Stakeholder communication

Formação académica

Bachelor’s degree or equivalent

Ferramentas

EDC systems

SAS programming

Microsoft Office

Descrição da oferta de emprego

iTRTech Group is offering a fully remote role for a Clinical Data Programmer/Manager (EDC). You will manage data lifecycle activities from study start-up to database lock, combining data management, programming, and system implementation tasks across HealthTech projects.

The ideal candidate brings 3+ years in clinical trials with EDC experience, SAS programming skills, and strong collaboration with sponsors and cross-functional teams, while maintaining regulatory compliance.