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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)

Company:

Syneos Health®

Location:

Remote – India

Job ID:

25101762

Updated On:

September 11, 2025


About Syneos Health

  • A fully integrated biopharmaceutical solutions organization.

  • 29,000 employees across 110 countries.

  • Partnered with 94% of FDA-approved drugs in the last 5 years and 95% of EMA authorized products.

  • Dedicated to career development, supportive management, training, peer recognition, and total rewards.

  • Follows a Total Self culture: diversity, authenticity, and belonging.


Job Summary

  • Acts as Lead Clinical Programmer to manage and support project deliverables/timelines.

  • Designs, writes, validates, and maintains software to meet study specifications.

  • Provides SME-level support for EDC systems, reporting tools, and integrations.

  • Manages external vendor issues and application performance.

  • Leads clinical programming activities across multiple studies (3–10 concurrently).


Core Responsibilities

  • Programming & Development

    • Use tools like Medidata Rave, Oracle Inform, Oracle OC/RDC, and SAS.

    • Design, validate, and maintain CRFs, edit checks, coding setups, imports/exports, listings, and reports.

    • Generate annotated CRFs and eCRF PDF reports.

  • Project & Team Leadership

    • Lead development activities and support project teams.

    • Manage project resources and alert management to delivery/resourcing needs.

    • Provide leadership, training, and guidance to clinical programming staff.

  • Quality & Compliance

    • Conduct senior review of deliverables for accuracy.

    • Attend sponsor audits and assist during in-progress audits.

    • Ensure deliverables meet specifications within timelines.

  • System Support

    • Monitor workflow alerts, errors, and system performance.

    • Provide second-tier help desk support.

    • Manage system integrations, application updates, and user acceptance testing.

  • Other Responsibilities

    • Review budgets, monitor scope of work, and manage change orders.

    • Attend Quick Start Camps (QSCs) for assigned studies.

    • Stay updated with literature, training, and professional meetings.


Qualifications

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

  • Experience:

    • 5+ years in clinical programming.

    • 4+ years in Custom Function Programming.

    • 3+ years in Database Migration/Post-DB changes (Impact Analysis).

    • Strong experience in Medidata Rave/iMedidata (CRF design, edit check programming, global libraries).

  • Skills:

    • Programming: PL/SQL, SAS, C#, VB (preferred).

    • Excellent communication, interpersonal, and problem-solving skills.

    • Ability to manage multiple priorities in a matrix environment.

    • Proficient in MS Office Suite.

    • Strong sponsor/client-facing skills.

  • Other:

    • Travel up to 25%.


Additional Information

  • This posting is for an upcoming opportunity (Talent Pipeline).

  • Equivalent skills/experience may be considered in place of listed qualifications.

  • Tasks/duties may be adjusted at the company’s discretion.

  • Committed to diversity, inclusion, and compliance with global legislation.