Principal Clinical Programmer (Veeva / Rave)
Updated: December 5, 2025
Location: Hyderabad, India (Hybrid)
Job ID: 25103365
Category: Clinical Programming | EDC | Biometrics
Syneos Health is a leading global biopharmaceutical solutions organization focused on accelerating clinical, medical affairs, and commercial outcomes. With operations in more than 110 countries and a workforce of 29,000, the company delivers integrated clinical development solutions designed to improve trial execution and enhance patient impact.
We continue to refine our Clinical Development model by placing both customers and patients at the center of every decision. Our teams work collaboratively to simplify processes, streamline operations, and advance high-quality clinical research.
Position Overview
The Principal Clinical Programmer (Veeva/Rave) is responsible for leading electronic data capture (EDC) programming activities for global clinical studies. This senior role manages the full lifecycle of database development tasks, including requirements gathering, CRF design, build, validation, UAT, deployment, and ongoing maintenance for Veeva EDC or Medidata Rave platforms.
This position requires deep expertise in EDC systems, strong technical leadership, and the ability to work in a fast-paced, cross-functional environment.
Key Responsibilities
EDC Design, Build, and Validation
Lead end-to-end EDC development in Veeva Clinical Data Management Suite or Medidata Rave.
Oversee eCRF design, edit checks, custom functions, derivations, and database validation activities.
Ensure database builds adhere to protocol requirements, global EDC standards, SDTM mapping requirements, and study timelines.
Perform impact assessments and implement enhancements across multiple phases of clinical trials.
Technical Oversight & Quality Assurance
Provide advanced technical expertise for EDC troubleshooting, system configuration, integration, and audit readiness.
Lead UAT planning, execution, issue tracking, and resolution in collaboration with data management and study teams.
Support database lock activities and ensure compliance with SOPs, regulatory requirements, and data quality standards.
Cross-functional Collaboration
Act as the primary point of contact for internal teams, sponsors, and CRO partners on EDC development matters.
Participate in project meetings, requirement workshops, kick-off sessions, and change control discussions.
Partner with Biometrics, Data Management, and Clinical Operations to ensure efficient system delivery.
Leadership and Process Development
Mentor junior programmers and contribute to technical training frameworks.
Support standardization activities, including libraries, templates, macros, and process optimization.
Provide subject matter expertise on Veeva CDMS, Rave, and emerging EDC technologies.
Organizational Contribution
Demonstrate initiative and continuously challenge existing processes to improve efficiency.
Participate in innovation efforts and technology transformation initiatives across the clinical programming function.
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Computer Science, Engineering, or a related field.
Minimum 8 years of clinical programming experience, with significant hands-on expertise in Veeva EDC and/or Medidata Rave.
Proven experience in EDC study build, metadata configuration, edit check programming, custom functions, dataset exports, and study maintenance.
Comprehensive understanding of clinical data standards, GCP, CDISC, SDTM, and regulatory compliance requirements.
Experience working on global Phase I–IV clinical trials in a CRO or sponsor environment.
Strong analytical skills with the ability to troubleshoot complex technical issues.
Excellent communication and documentation skills, with strong stakeholder coordination experience.
Experience in Functional Service Provider (FSP) or hybrid sponsor models is an advantage.
Why Join Syneos Health
Exposure to 94 percent of all Novel FDA-approved drugs and 95 percent of EMA-authorized products over the past five years.
Opportunity to contribute to more than 200 clinical studies across 73,000 global sites.
Structured learning programs and career progression pathways with technical and therapeutic area training.
A collaborative culture built on diversity, inclusion, and the organization’s Total Self philosophy.
Recognition programs, supportive leadership, and a workplace focused on employee well-being and professional growth.
Learn more about the organization at syneoshealth.com.
Additional Information
The responsibilities listed above are not exhaustive. Additional tasks may be assigned based on business needs. Qualifications may vary depending on equivalent education or relevant experience. Nothing in this description constitutes an employment contract. Syneos Health complies with global employment regulations, including the EU Equality Directive and the Americans with Disabilities Act, and provides reasonable accommodations where appropriate.
How to Apply
Submit your application through the Syneos Health career portal or join the Talent Network to receive updates on future opportunities.
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