Remote Senior Clinical Database Programmer, Veeva CDMS

Pulmovant; United States; Remote; USD 120,000 - 180,000; Full time

Job summary

Pulmovant is seeking a Senior Clinical Database Programmer to provide technical oversight of EDC builds in Veeva CDMS and to support vendor data transfers. The role requires 6–8 years in clinical data programming within an FDA-regulated environment and strong Veeva CDMS expertise.

Responsibilities include coordinating with the Lead Clinical Data Manager, managing post-production changes, and ensuring data integrity across vendor data transfers and EDC integrations.

Qualifications

• 6–8 years of clinical data programming in FDA-regulated environment.
• Hands-on experience building/maintaining databases in Veeva CDMS.
• Experience with vendor data transfers and data integrations.
• Experience with EDC builds and post-production changes.

Responsibilities

• Provide technical oversight of EDC build and maintenance in Veeva CDMS.
• Review build requirements with the Lead Clinical Data Manager.
• Assess impact of post-production changes on data and deliverables.
• Review Veeva CDMS and DQS release notes for impacts to studies.
• Provide hands-on technical support to vendors and study teams.

Skills

Veeva CDMS

Education

Bachelor’s degree in Biology, Chemistry, Physics, Computer Science, Information Technology, Biotechnology, Bioinformatics

Tools

Veeva CDMS

Veeva DQS

Job description

Pulmovant is seeking a Senior Clinical Database Programmer to provide technical oversight of EDC builds in Veeva CDMS and to support vendor data transfers. The role requires 6–8 years in clinical data programming within an FDA-regulated environment and strong Veeva CDMS expertise.

Responsibilities include coordinating with the Lead Clinical Data Manager, managing post-production changes, and ensuring data integrity across vendor data transfers and EDC integrations.