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Principal Clinical Programmer (Rave/Veeva)

Syneos Health
Syneos Health
8-9 years
preferred by company
10 Dec. 26, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Principal Clinical Programmer (Rave / Veeva EDC)

Job ID: 25103366
Location: Gurugram, India (Hybrid)
Employment Type: Full-Time
Category: Clinical Programming | Clinical Data Management | EDC Systems
Experience Required: 8–9 years in Clinical Programming
Updated On: December 19, 2025


About the Organization

Syneos Health® is a leading, fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success across clinical development, medical affairs, and commercialization. With operations spanning more than 110 countries and a workforce of over 29,000 professionals, Syneos Health partners with biopharmaceutical innovators to bring therapies to patients faster.

Our patient-centric Clinical Development model emphasizes innovation, efficiency, and collaboration. Whether operating in a Functional Service Provider (FSP) or Full-Service model, teams work in agile environments focused on delivering high-quality outcomes that improve lives globally.


Role Overview

The Principal Clinical Programmer (Rave / Veeva) serves as a senior technical subject matter expert responsible for leading end-to-end clinical programming activities across single studies and large, complex programs. This role combines hands-on EDC development expertise with leadership, vendor oversight, and cross-functional collaboration.

The position is ideal for experienced clinical programmers with strong Medidata Rave or Veeva EDC expertise, advanced database build experience, and the ability to manage multiple studies while mentoring junior team members.


Key Responsibilities

Clinical Programming & EDC Leadership

  • Act as subject matter expert for core clinical systems including Medidata Rave, Veeva EDC, Oracle OC/RDC, Oracle Inform, SAS, and related reporting and migration tools

  • Design, build, validate, and maintain EDC databases including eCRFs, edit checks, custom functions, migrations, imports, and exports

  • Lead end-to-end clinical programming deliverables aligned with annotated CRFs and study specifications

  • Proactively monitor applications for workflow alerts, system errors, performance issues, and troubleshoot defects

Project & Program Management

  • Lead and coordinate clinical programming activities across multiple concurrent studies (typically 5–20 studies depending on scope)

  • Serve as programming lead on project teams, ensuring timelines, scope, and quality standards are met

  • Communicate risks, issues, and resourcing needs to project management and escalate proactively

  • Review study budgets, track metrics, manage scope-to-work alignment, and support change order execution

Quality, Compliance & Audits

  • Perform senior-level reviews of program-level and multi-study deliverables to ensure accuracy and regulatory compliance

  • Support sponsor audits, internal audits, and in-progress inspections

  • Contribute to SOPs, work instructions, and continuous process improvement initiatives

Leadership, Mentorship & Vendor Oversight

  • Provide technical leadership, mentoring, and training to clinical programmers across programs

  • Oversee work allocation, workload balancing, and quality reviews for junior and lead programmers

  • Manage external application vendors, monitor SLAs, and serve as an escalation point

  • Supervise system upgrades, integrations, and new module implementations for hosted EDC platforms


Education & Experience Requirements

Required

  • Bachelor’s degree in a relevant discipline (Master’s degree preferred) or equivalent combination of education and experience

  • 8–9 years of hands-on experience in clinical programming within a CRO or pharmaceutical environment

  • End-to-end Rave OR Veeva EDC experience, including database build and study implementation

  • Strong experience with:

    • Study and database builds

    • eCRF design

    • Edit check programming

    • Data migrations and post-production changes (PPC)

    • Custom function programming (for Rave EDC)


Preferred Qualifications

  • Experience working in matrixed, global project environments

  • Exposure to programming languages such as PL/SQL, SAS, C#, or VB

  • Strong stakeholder management experience with sponsors and internal teams

  • Ability to manage multiple priorities in fast-paced clinical development programs

  • Willingness to travel up to 25% as project needs require


Key Skills & Competencies

  • Advanced EDC systems expertise (Rave / Veeva)

  • Strong analytical and problem-solving skills

  • Excellent written and verbal communication skills

  • Leadership and mentoring capability

  • High attention to detail and commitment to data quality

  • Proficiency in Microsoft Office applications


Why Join Syneos Health?

  • Work with a global organization involved in over 94% of recent FDA novel drug approvals

  • Collaborate across diverse teams delivering studies at scale across regions and therapeutic areas

  • Access structured career development, technical training, and leadership progression

  • Be part of an inclusive, people-first culture focused on growth, innovation, and impact


Role Summary

The Principal Clinical Programmer leads clinical programming strategy and execution across complex clinical programs, ensuring high-quality EDC solutions, regulatory compliance, and on-time delivery. As a senior technical expert, this role supports clinical data management and programming teams while driving innovation, mentoring talent, and partnering closely with sponsors and vendors.