Senior Clinical Programmer (Veeva)
Updated: April 28, 2025
Job ID: 25003246
Location: India-Asia Pacific – IND-Home-Based
About Syneos Health:
Syneos Health® is a fully integrated biopharmaceutical solutions organization committed to accelerating customer success. With a presence in over 110 countries and 29,000+ employees, we partner with clients through both Functional Service Provider and Full-Service models. At Syneos Health, we unite medical, clinical, and commercial capabilities to bring life-changing therapies to market.
Why Join Us:
Opportunities for career progression, technical upskilling, and therapeutic training
Supportive leadership and recognition programs
Total Self culture that promotes inclusion and authenticity
Work that makes a global impact
Job Responsibilities:
Utilize tools such as Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, and others to develop and validate software in line with project specifications and standard procedures
Produce and maintain key documentation (specifications, programs, validation reports) supporting annotated CRFs, database creation, coding, edit checks, imports/exports, listings, and reports
Coordinate and lead clinical programming projects, providing updates on deliverables, scope, budget, and risks
Support Project Analysts, Data Managers, and other staff by guiding development and validation of CRFs, databases, edit checks, etc.
Serve as SME for application administration on platforms such as Oracle Inform, MDSOL Rave, SAS, and related tools
Review and ensure high quality of study-level, program-level, and multi-study deliverables
Participate in sponsor audits and assist in in-progress audits
Review budgets, monitor scope vs. actual work, and execute change orders when required
Monitor workflow alerts, errors, and performance issues, providing tier-2 help desk support
Perform system integration, application upgrades, and UAT
Offer leadership and training to junior team members and collaborate across teams for finalizing specifications
Attend project meetings and departmental review sessions, acting as lead Clinical Programmer for assigned studies
Manage programming activities across 3–10 concurrent studies, depending on scope and resource needs
Stay updated on developments in clinical programming and data management through continuous learning
Required Qualifications:
Bachelor’s degree or equivalent combination of education and experience
Strong communication and interpersonal skills
Ability to work effectively with sponsors and internal stakeholders at all levels
Experience managing multiple priorities in a dynamic environment
Familiarity with matrix-structured organizations preferred
Proficient in MS Office (Word, Excel, PowerPoint), email, and voicemail systems
Experience with programming languages (PL/SQL, SAS, C#, VB) preferred
Willingness to travel up to 25% as needed
About Syneos Health Clinical Impact:
Supported 94% of all FDA-approved novel drugs in the past 5 years
Partnered on over 200 studies across 73,000 sites with 675,000+ trial patients
Driven by initiative, innovation, and a commitment to challenge the status quo
Additional Information:
This job description is not exhaustive. Syneos Health may amend or assign new responsibilities without prior notice. Equivalent qualifications may be considered, and no element here creates a contractual obligation. All job requirements comply with applicable laws, including disability accommodations and equal opportunity principles.
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