Senior Clinical Programmer (Rave/Veeva)
Location: Gurugram, India (Hybrid) | Job ID: 25103879 | Employment Type: Full-Time
About Syneos Health
Syneos Health® is a global, fully integrated biopharmaceutical solutions organization dedicated to accelerating drug development and delivering meaningful patient outcomes. Our Clinical Development model centers on the patient and customer, leveraging innovative solutions across clinical, medical affairs, and commercial functions.
We operate in Functional Service Provider (FSP) partnerships and Full-Service environments, empowering teams to deliver high-quality clinical programming solutions across the drug development lifecycle.
Role Overview
The Senior Clinical Programmer (Rave/Veeva) will lead and execute clinical programming activities across multiple studies. This role combines hands-on technical expertise with leadership responsibilities, ensuring timely, accurate, and compliant delivery of clinical trial data, eCRFs, and reporting. The ideal candidate will have experience in EDC build, edit check programming, migration activities, and custom functions with strong proficiency in Rave/Veeva platforms.
Key Responsibilities
Develop, validate, and maintain software and scripts to support annotated CRFs, database creation, coding configuration, edit checks, import/export processing, listings, and custom reports.
Lead clinical programming efforts for 3–10 concurrent studies, providing technical guidance, mentorship, and supervision to junior programmers.
Review and ensure accuracy of study-level and multi-study deliverables, supporting sponsor audits and internal quality checks.
Monitor applications for workflow alerts, system errors, and performance issues; provide troubleshooting and second-tier support.
Participate in project meetings, Quick Start Camps (QSCs), and departmental reviews; communicate project risks, scope changes, and status updates.
Collaborate with cross-functional teams including Data Management, Project Analysts, and clinical leads to ensure data integrity and compliance.
Support system integration activities, application updates, and user acceptance testing.
Contribute to SOP updates, process improvements, and documentation standards.
Qualifications & Experience
Bachelor’s degree in Life Sciences, Computer Science, or equivalent; Master’s preferred.
5+ years of clinical programming experience with proven expertise in Rave/Veeva EDC platforms.
Minimum 4 years of Custom Function programming experience.
Minimum 3 years of experience in migration activities including impact analysis post-database changes.
Experience with edit check programming, dynamic edits, global libraries, and generating eCRF PDF reports.
Strong interpersonal and communication skills; ability to interface with sponsors and internal stakeholders at all levels.
Ability to manage multiple priorities in a dynamic, matrix-structured environment.
Proficiency in Microsoft Office Suite; knowledge of programming languages such as PL/SQL, SAS, C#, or VB preferred.
Willingness to travel up to 25% as needed.
Why Syneos Health
Opportunity to work on global clinical trials across diverse therapeutic areas.
Career development, mentorship, and technical training programs.
Inclusive, collaborative work culture emphasizing diversity, equity, and belonging.
Exposure to cutting-edge clinical programming technologies and EDC platforms.
Apply Now
Advance your career as a Senior Clinical Programmer (Rave/Veeva) at Syneos Health and lead high-impact clinical programming initiatives supporting global drug development programs.
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