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Sr Clinical Programmer (Edc Programming-Rave/Veeva)

5+ years
Not Disclosed
10 Sept. 19, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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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