Senior Data Management Programmer

Main Responsibilities:

·Design, build, maintain and close clinical trial databases using EDC and paper-based systems.

·Develop and maintain CDISC-compliant data standards, mappings and documentation.

·Program data extractions, listings, edit checks, protocol deviation reports and custom functions.

·Implement and manage CRF and non-CRF data handling procedures.

·Test databases and validation procedures to ensure data integrity and quality.

·Monitor data management activities across multiple clinical studies.

·Identify process improvement opportunities and support implementation of innovative technologies.

·Support programming activities for regulatory submissions and audit requirements.

·Provide technical guidance and mentorship to team members.

Qualifications and Experience:

• Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required;

·Associate degree, Bachelor degree or equivalent in Mathematics, Informatics, Engineering or a related discipline.

·Minimum 5 years of programming experience within Clinical Data Management in a pharmaceutical company or CRO.

·Strong understanding of CDISC and SDTM standards.

·Hands-on experience with Clinical Data Management Systems, EDC platforms and data reporting tools.

·Knowledge of ICH-GCP, 21 CFR Part 11 and global clinical research regulations.

·Advanced English language skills.

·Clinical database design and validation.

·Database build, derivations, coding and discrepancy management.

·Clinical data reporting and extraction programming.

·Development of global data standards and mappings.

·Microsoft Office and Windows environment proficiency.