Job Title:
Sr Clinical Programmer (EDC Programming – Rave/Veeva)
Updated: September 11, 2025
Location: IND – Hyderabad
Job ID: 25101762
About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success by combining clinical, medical affairs, and commercial insights.
29,000 employees across 110 countries
Partnered with 94% of FDA-approved drugs & 95% of EMA-authorized products in the last 5 years
Delivered 200+ studies across 73,000 sites with 675,000+ trial patients
We are committed to:
Career growth – training, progression, and mentorship
Total Self culture – inclusion, diversity, authenticity
Innovation – simplifying processes, driving productivity
Work Here Matters Everywhere.
Job Summary
As a Sr Clinical Programmer, you will:
Serve as lead programmer managing project deliverables and timelines.
Design, write, validate, and maintain software for data capture and processing.
Act as a first-level SME supporting EDC, reporting, and data management staff.
Monitor applications for errors and performance issues.
Collaborate with external vendors for application issues, integrations, and implementations.
Core Responsibilities
Use primary tools (Medidata Rave, Oracle OC/RDC, Oracle Inform, SAS, etc.) to design, develop, validate, and maintain applications.
Generate & maintain documentation: specifications, annotated CRFs, database creation, edit checks, import/export setups, listings, custom reports.
Coordinate programming activities across multiple studies; provide updates on timelines, scope, and budgets.
Provide technical support for programming staff and project teams.
Act as SME for core applications: Oracle Inform, Rave, RDC, SAS, and reporting tools.
Ensure high-quality deliverables through senior-level review and audit support.
Support change orders, budgets, and scope monitoring.
Handle application administration, workflow alerts, UAT, and integrations.
Provide training, mentorship, and guidance to peers and junior staff.
Lead 3–10 concurrent studies (depending on scope).
Maintain expertise through continuous learning and professional development.
Qualifications
Education: Bachelor’s degree preferred (or equivalent experience).
Experience:
5+ years total experience in clinical programming.
Strong experience in Custom Function Programming (4+ years).
3+ years in Migration/Post-DB change activities with impact analysis.
Hands-on with Medidata Rave/iMedidata – eCRF design, edit checks, dynamic edits, Global Libraries, and eCRF PDF reports.
Experience leading Clinical Study Design & Specification documentation.
Technical Skills:
Programming: PL/SQL, SAS, C#, VB (preferred).
Tools: Microsoft Office Suite, reporting tools, migration mentor/review.
Soft Skills:
Strong communication & interpersonal skills.
Ability to manage multiple priorities in a matrix environment.
Experience collaborating with sponsors and internal stakeholders.
Other:
Travel: Up to 25% as needed.
Additional Information
Role is part of our talent pipeline for upcoming opportunities.
Tasks listed are not exhaustive; other responsibilities may be assigned.
Equivalent skills/experience may be considered.
Fully compliant with EU Equality Directive & ADA (reasonable accommodations provided).
Application
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