Job Title: Senior Clinical Programmer (Veeva)
Updated: April 28, 2025
Location: India (Home-Based, Asia-Pacific)
Job ID: 25003246
Company: Syneos Health
Position Summary
Syneos Health is seeking a Senior Clinical Programmer with expertise in Veeva systems and clinical data platforms such as Medidata Rave, Oracle Inform, and SAS. This position will be responsible for designing, programming, validating, and supporting clinical trial data systems and tools to ensure data integrity, regulatory compliance, and high-quality deliverables. The ideal candidate is technically skilled, organized, and capable of leading multiple concurrent programming projects within a global CRO environment.
Key Responsibilities
Design, program, validate, and maintain clinical databases using Medidata, Oracle, SAS, and Veeva tools.
Develop annotated CRFs, data edit checks, data imports/exports, listings, and custom reports.
Lead and coordinate programming activities across 3–10 concurrent studies.
Provide technical support to clinical programming, data management, and project teams.
Serve as subject matter expert for clinical data systems and conduct UAT, upgrades, and integration activities.
Monitor workflow alerts, system issues, and application performance; provide second-tier helpdesk support.
Review and provide input on budgets, manage scope changes, and lead change order execution.
Deliver internal training, mentor junior programmers, and contribute to departmental knowledge sharing.
Participate in project and audit meetings, sponsor interactions, and ensure study milestones are met.
Required Qualifications
Education: Bachelor’s degree (science, technology, or related field) or equivalent combination of education and experience.
Experience:
Clinical data programming experience with platforms like Medidata Rave, Oracle RDC/Inform, and SAS.
Programming language skills in PL/SQL, SAS, C#, or VB preferred.
Strong background in clinical data management and system validation.
Experience working in a matrix environment and managing cross-functional project resources.
Skills:
Excellent communication, project management, and documentation skills.
Ability to multitask and deliver under tight deadlines.
Proficiency in Microsoft Office (Word, Excel, PowerPoint).
Willingness to travel up to 25%.
Why Join Syneos Health
Collaborate with world-class teams contributing to 94% of FDA novel drug approvals.
Be part of a culture that fosters innovation, diversity, and personal growth.
Thrive in a flexible remote working environment while making a meaningful impact in global health.
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