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Sr Clinical Programmer (Edc Programming-Rave/Veeva)

5+ years
Not Disclosed
10 Sept. 24, 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

Sr Clinical Programmer (EDC Programming – Rave/Veeva)

Location: Hyderabad, India
Job ID: 25101762
Updated: September 11, 2025


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating clinical development and improving patient outcomes.

  • Employees: 29,000 across 110 countries

  • Experience: 94% of Novel FDA-approved drugs, 95% EMA-authorized products, 200+ studies, 73,000 sites, 675,000+ trial patients

  • Culture: Total Self culture promoting diversity, authenticity, career growth, and inclusion


Job Overview

The Sr Clinical Programmer leads clinical programming activities for EDC systems (Rave/Veeva), ensuring project deliverables and timelines are met. This role serves as the technical SME for EDC programming, database builds, reporting, and data processing, providing support to project teams and data management staff.


Key Responsibilities

  • Lead clinical programming for multiple studies (3–10 concurrently).

  • Design, write, validate, and maintain software and applications supporting EDC, data capture, and processing.

  • Develop specifications, programs, edit checks, import/export setups, listings, and custom reports.

  • Provide first-level technical support and guidance for clinical programming and EDC tools.

  • Monitor applications for system errors, workflow alerts, and performance issues.

  • Collaborate with project teams, clients, and vendors for application integrations, issue resolution, and implementations.

  • Review study budgets, monitor scope of work, and support change order execution.

  • Participate in project meetings, departmental reviews, Quick Start Camps (QSCs), and sponsor audits.

  • Mentor and provide training to clinical programming staff.

  • Maintain up-to-date knowledge of clinical programming, EDC systems, and clinical data management best practices.


Required Skills & Qualifications

  • Education: Bachelor’s degree preferred, or equivalent experience.

  • Experience: 5+ years in clinical programming; 4+ years in Custom Function Programming; 3+ years in Migration (Post-DB Changes) activities.

  • EDC Expertise: Medidata Rave and iMedidata, edit checks, dynamic edits, global libraries, eCRF PDF report generation.

  • Technical Skills: PL/SQL, SAS, C#, VB (preferred); strong Microsoft Office proficiency.

  • Project Skills: Lead study design and database build, manage multiple priorities in dynamic environment.

  • Communication: Excellent interpersonal, written, and verbal skills.

  • Travel: Up to 25% as required.

  • Additional: Experience in matrix-structured environments preferred; ability to interact effectively with sponsors and internal stakeholders.


Additional Information

  • Tasks and responsibilities may be adjusted by the company as needed.

  • Equivalent experience, skills, or education may be considered.

  • Compliance with ADA and diversity/inclusion policies.

  • Expressing interest adds you to Syneos Health’s talent pipeline for upcoming opportunities.