Senior Clinical Database Programmer

Job Summary

Offering a remote full-time opportunity, the Senior Clinical Database Programmer will provide technical oversight of EDC build and maintenance in Veeva CDMS, support vendor data transfers, and collaborate with the Lead Clinical Data Manager to ensure data integrity and compliance in clinical studies.

Key responsibilities

• Provide technical oversight of EDC build and maintenance in Veeva CDMS, including review of specifications and deliverables
• Support vendor data transfers for external data and ensure integration with the EDC is implemented and tested
• Assess the impact of post-production changes on existing data and coordinate with IT for necessary updates

Required qualifications

• Bachelor's degree in a relevant field such as Biology, Chemistry, or Computer Science
• 6 to 8 years of clinical data programming experience in an FDA regulated environment
• At least 4 years of hands-on experience with Veeva CDMS, including building and maintaining databases
• Experience with vendor data transfers and authoring transfer specifications
• Strong knowledge of data management practices within the ICH GCP and regulatory environment