Senior Clinical Programmer (Medidata RAVE & Veeva CDB Admin) – Hyderabad, Hybrid
Location: Hyderabad, India (Hybrid)
Employment Type: Full-Time
Job ID: 25103878
Experience Required: 5–8 Years
Industry: Biopharmaceuticals | Clinical Data Management | EDC Administration
About Syneos Health
Syneos Health® is a leading global biopharmaceutical solutions company, integrating clinical development, medical affairs, and data science to accelerate therapeutic delivery. Our mission is to simplify clinical trials, enhance data quality, and improve patient outcomes.
We operate across 110 countries with over 29,000 employees, supporting innovative clinical programs from study start-up to submission. Our Functional Service Provider (FSP) model ensures agile, scalable, and compliant delivery for complex global trials.
Role Overview
We are seeking a Senior Clinical Programmer with expertise in Medidata RAVE and Veeva CDB administration. The role is responsible for governance, configuration, lifecycle management, and operational oversight of global EDC environments. This includes managing RAVE study URLs, Veeva CDB ingestion pipelines, harmonization, automated cleaning, and downstream data delivery.
This position serves as a Subject Matter Expert (SME), providing guidance to clinical programmers, data managers, and cross-functional study teams to ensure high-quality, compliant, and audit-ready data management.
Key Responsibilities
Medidata RAVE URL Administration:
Configure and manage RAVE environments (DEV, UAT, PROD, TRAINING) across global studies
Enforce naming conventions, lifecycle standards, roles/permissions, and integrations
Perform environment readiness checks and validation for secure study operations
Develop and maintain SOPs, Work Instructions, and automated workflows for environment provisioning
Serve as first-line SME for URL issues, coordinating escalations and CAPA activities
Partner with Clinical Programming, Data Science, RTSM, and vendor teams for study readiness
Veeva CDB Administration:
Administer Veeva CDB, Vault CDMS, and Data Workbench, including user access, study roles, and permissions
Manage ingestion of multi-source clinical datasets (EDC, labs, eCOA/ePRO, imaging, RTSM)
Validate data integrity, harmonize study datasets, and support automated query management
Configure CQL pipelines, no-code/low-code transformations, and API integrations for downstream data delivery
Monitor study health, data readiness, query status, and provide reporting to clinical teams
Mentor junior administrators and ensure compliance with GxP, GCP, 21 CFR Part 11, GDPR
Stakeholder Engagement & Compliance:
Collaborate with global study teams to align environment and CDB strategies with timelines and milestones
Maintain audit-ready documentation and provide updates for governance forums
Support platform-related escalations, troubleshooting, and technical guidance
Required Qualifications
5+ years of clinical data management, EDC administration, or clinical programming experience
3+ years hands-on experience with Medidata RAVE environment management
Strong expertise in Veeva CDB, Vault CDMS, Data Workbench, and clinical data pipelines
Deep understanding of EDC integrations, automated data cleaning, query management, and downstream data delivery
Working knowledge of GxP, GCP, 21 CFR Part 11, GDPR, and validation/CSV principles
Experience with CQL, APIs, and automation/scripting for environment and data management
Excellent analytical, problem-solving, communication, and stakeholder management skills
Preferred Qualifications:
Familiarity with SDTM, ADaM, or clinical programming languages (SAS, Python, R)
Exposure to global governance committees, SOP authorship, and CAPA leadership
Experience in multi-country trials, system integrations, and cloud-based EDC/CDMS platforms
Why Join Syneos Health
Lead global clinical trials across diverse therapeutic areas
Work in a collaborative, innovative, and inclusive environment
Access career development, mentorship, and advanced training
Influence process improvements, automation initiatives, and high-quality trial data delivery
Be part of a company that has worked with 94% of Novel FDA Approved Drugs and 95% of EMA Authorized Products over the past 5 years
Equal Opportunity Employer
Syneos Health is an equal opportunity employer, welcoming candidates of diverse backgrounds. Transferable skills and equivalent experience are considered, and reasonable accommodations are provided in compliance with applicable laws.
Apply Now
Join Syneos Health as a Senior Clinical Programmer (Medidata RAVE & Veeva CDB Admin) to drive data integrity, compliance, and operational excellence in global clinical trials.
Gujarat :
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Pondicherry (Puducherry) |Jharkhand :
Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Wisconsin :
Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Paris | Lyon |South Africa :
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