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Principal Clinical Programmer (Rave/Veeva)

8+ years
Not Disclosed
10 July 30, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Principal Clinical Programmer (Rave/Veeva) – Remote, India

Job Summary

Syneos Health is seeking a seasoned Principal Clinical Programmer with deep expertise in Rave and/or Veeva EDC systems. This remote role is ideal for experienced professionals with a strong background in clinical data management, CRF design, edit check programming, and end-to-end clinical database build. This position leads large-scale clinical programming projects, oversees multiple studies concurrently, and contributes significantly to trial quality and delivery across global programs.


Key Responsibilities

  • Act as SME in Medidata Rave, Oracle OC/RDC, Veeva Vault, SAS, and related platforms.

  • Lead EDC development: eCRF build, edit check programming, custom functions, migrations, and PPC.

  • Coordinate and oversee delivery across up to 20 concurrent studies.

  • Provide technical support, troubleshoot system issues, and ensure application performance.

  • Supervise vendor deliverables and track performance against SLAs.

  • Conduct system upgrades, UAT, documentation, and user training.

  • Guide study teams, attend QSCs, and collaborate in bid defense meetings.

  • Participate in SOP reviews and department process improvements.

  • Mentor junior programmers and contribute to performance evaluations.

  • Support audits, budget reviews, and change order management.


Required Skills & Qualifications

  • Bachelor’s degree required; Master’s preferred (clinical, tech, or data-related fields).

  • Minimum 8 years’ experience in end-to-end clinical programming, with strong EDC build expertise.

  • Hands-on expertise with Medidata Rave, Veeva Vault EDC, custom functions, migrations, and edit checks.

  • Prior lead programmer experience on multiple concurrent studies.

  • Experience with PL/SQL, SAS, C#, or VB is a plus.

  • Strong communication, leadership, and cross-functional collaboration skills.

  • Experience working in CRO or pharma IT environment preferred.

  • Ability to manage teams and mentor others in a matrix setting.

  • Up to 25% travel may be required.


Perks & Benefits

  • 100% Remote Work Opportunity (India-based)

  • Competitive salary (not specified; based on experience)

  • Career development & upskilling programs

  • Employee recognition and total rewards system

  • Inclusive “Total Self” work culture

  • Exposure to global clinical trials and leading technologies

  • Opportunity to work on FDA/EMA drug approvals


Company Overview

Syneos Health is a leading global CRO that partners with biopharma companies to deliver results across clinical development, medical affairs, and commercialization. With over 29,000 employees in 110 countries, Syneos has supported 94% of all novel FDA approvals in recent years. Join us to contribute to meaningful trials that drive innovation in global healthcare.


Work Mode: Remote (India-based)
Experience Level: Senior (8+ years)
Job Type: Full-Time, Permanent


Apply Now

Ready to lead complex clinical programs and innovate in a fast-paced biopharma environment? Apply now and shape the future of global clinical research with Syneos Health.