Remote Clinical Data Programmer (Medidata Rave)

Alimentiv; Lisboa; On-site; EUR 42,000 - 66,000; Full time

Benefits offered by this job

Education Reimbursement

Monthly Cell Phone Allowance

Office setup allowance

Mentorship program

Job summary

Alimentiv is seeking a dedicated Clinical Database Programmer to support the development, testing and maintenance of EDC systems for clinical trials. You will build study databases, configure eCRFs, and ensure data integrity across projects.

You will work within a collaborative team, explore AI-driven solutions, and help drive continuous improvements in study development and operational efficiency. This is a full-time role based in Lisbon, Portugal.

Qualifications

• Degree or diploma in Computer Science, Information Technology or related field.
• Experience in clinical database development and EDC programming.
• Experience within a CRO or pharmaceutical environment is desirable.
• Knowledge of eCRFs, edit checks, DB testing and data management processes.
• Understanding of programming principles and database development.

Responsibilities

• Design, build, test and maintain clinical study databases within EDC systems.
• Develop and configure eCRFs, edit checks and study-specific database requirements.
• Support data transfers, integrations and database validation activities.
• Troubleshoot technical issues and provide EDC study support.
• Collaborate with Data Management and project teams to ensure delivery.
• Contribute to automation and AI-driven improvements.

Skills

Clinical data management

EDC systems

Analytical thinking

Communication

Team collaboration

Education

CS/IT degree

Tools

Medidata Rave

C# programming

Job description

Alimentiv is seeking a dedicated Clinical Database Programmer to support the development, testing and maintenance of EDC systems for clinical trials. You will build study databases, configure eCRFs, and ensure data integrity across projects.

You will work within a collaborative team, explore AI-driven solutions, and help drive continuous improvements in study development and operational efficiency. This is a full-time role based in Lisbon, Portugal.