Senior Clinical Programmer – Rave & Veeva CDB Administrator
Updated: Yesterday
Location: Gurgaon, Haryana, India
Job ID: 25103878-OTHLOC-5206-2DH
Employment Type: Full-Time
About Syneos Health®
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. By combining expertise across clinical development, medical affairs, and commercialization, Syneos Health delivers innovative solutions that address today’s complex clinical and regulatory challenges.
With operations in over 110 countries and a strong patient-centric Clinical Development model, Syneos Health partners with sponsors through Functional Service Provider (FSP) and Full-Service engagements to accelerate the delivery of life-changing therapies worldwide.
Position Overview
The Senior Clinical Programmer – Rave & Veeva CDB Administrator is a senior subject matter expert responsible for end-to-end administration, governance, and lifecycle management of Medidata RAVE environments and Veeva Clinical Database (CDB) platforms. This role supports global clinical trials by ensuring secure, compliant, and efficient clinical data systems, enabling seamless study startup, execution, and closeout.
The position requires strong expertise in EDC platform administration, multi-source clinical data ingestion, automation, and regulatory compliance, with close collaboration across Biometrics, Clinical Programming, Data Management, Study Operations, QA/CSV, and vendors.
Key Responsibilities
Medidata RAVE URL Administration (SME Level)
Environment Governance and Configuration
Govern and manage RAVE environments (DEV, UAT, PROD, TRAINING) across global FSO Biometrics studies
Define and enforce standards for URL creation, naming conventions, migrations, cloning, and archival
Perform environment readiness checks including roles, permissions, system settings, and integrations
Author and maintain SOPs and work instructions related to environment provisioning and change control
Support SaaS version impact assessments and environment validation activities
Access Management, Compliance, and Quality
Govern role-based access control (RBAC) and enforce least-privilege security principles
Ensure compliance with GxP, GCP, 21 CFR Part 11, GDPR, and data privacy requirements
Maintain audit-ready documentation including approvals, validation evidence, and change logs
Lead issue triage, root cause analysis, and CAPA activities related to environment deviations
Stakeholder Collaboration and Process Optimization
Act as primary escalation point for environment and URL-related issues
Coordinate with Medidata support and internal platform owners
Drive process improvements and automation initiatives to reduce provisioning cycle times
Mentor junior administrators and contribute to knowledge management initiatives
Veeva Clinical Database (CDB) Administration
Platform Administration and Study Enablement
Administer Veeva CDB, Vault CDMS, EDC, and Data Workbench including user access, roles, and security
Enable ingestion pipelines and common study backbone mapping for multi-source clinical data
Support study setup and configuration across internal and external data sources
Data Ingestion, Harmonization, and Cleaning
Monitor and manage durable ingestion engines for EDC, labs, eCOA/ePRO, imaging, RTSM, and external vendors
Validate incoming datasets and troubleshoot ingestion, metadata, and alignment issues
Oversee automated discrepancy detection, query generation, and centralized query management
Clinical Programming and Automation Support
Support data transformation using Veeva Clinical Query Language (CQL)
Enable no-code/low-code and API-driven exports for downstream programming and reporting systems
Support automated data quality checks and real-time study data review
Monitoring, Reporting, and User Support
Track study data health, query status, and data readiness dashboards
Provide regular updates on data lock preparedness and operational metrics
Conduct training sessions for study teams and support escalations with Veeva Product Support
Required Qualifications and Experience
Education
Bachelor’s degree in Life Sciences, Computer Science, Biostatistics, or a related discipline
Equivalent practical experience will be considered
Experience
5–8 years of experience in clinical systems administration, EDC, clinical programming, or data management
Minimum 3 years of hands-on experience with Medidata RAVE environment administration
At least 2–3 years of experience with Veeva CDB / CDMS / EDC platforms
Proven experience managing multi-source clinical trial data and global studies
Technical Skills
Strong understanding of RAVE architecture, environment lifecycle, and integrations (Coder, RTSM, CDS)
Hands-on expertise with Veeva CDB ingestion pipelines, Data Workbench, and query workflows
Working knowledge of CQL or similar data transformation/query languages
Experience supporting API-based integrations (REST APIs, JSON, Postman preferred)
Compliance and Soft Skills
Strong understanding of CSV, audit trails, and regulatory compliance standards
Excellent documentation, communication, and stakeholder management skills
Ability to manage multiple global studies and work across time zones
Preferred Qualifications
Experience with automation, scripting, or APIs for environment provisioning
Exposure to SAS, Python, or R for clinical data workflows
Familiarity with SDTM concepts and downstream data structures
Experience authoring SOPs and participating in global governance committees
Why Join Syneos Health?
Career growth through structured learning and leadership development
Exposure to large-scale, global clinical trials and advanced CDMS platforms
Collaborative, inclusive, and high-performance work culture
Opportunity to contribute to studies supporting novel FDA- and EMA-approved therapies
Over the past five years, Syneos Health has supported:
94% of novel FDA-approved drugs
95% of EMA-authorized products
200+ studies across 73,000 sites and 675,000+ trial participants
Additional Information
Responsibilities may evolve based on business and project needs
Equivalent education and experience combinations will be considered
This job description does not constitute an employment contract
Syneos Health is an equal opportunity employer and complies with all applicable employment and accessibility regulations
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