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Tier-1 employer plus Bengaluru metro and a data role increases competition, despite niche Veeva requirement.
Clinical trials domain, Veeva expertise, and regulatory requirements limit cross-industry transferability.
Mandatory clinical-data tooling, regulatory expertise, and domain-specific systems make filters stringent.
Design, develop, validate, and maintain clinical data review solutions and reporting tools including CDB Checks, Listings, Reconciliations, Medical/Safety Reviews, PD Reviews, and CDMS reporting.
Provide technical oversight on solution architecture, coding standards, validation practices, and ensure quality compliance for clinical data acquisition.
Support complex data reconciliations across multiple data sources and mentor programming teams while collaborating with Data Management and cross-functional stakeholders to meet study milestones and regulatory requirements.
Advanced experience in Clinical Data Management or Clinical Data Review Programming or related clinical systems roles.
Strong expertise in Veeva CDB, Veeva CDMS Reports, Domino, R, Python, SQL, and knowledge of clinical data standards.
Deep understanding of clinical trial processes, data review methodologies, reconciliation processes, and regulatory requirements.
Work Experience Required: Not explicitly mentioned in the JD.
Experienced in leading complex technical initiatives within clinical data acquisition and able to influence cross-functional teams and stakeholders.
Technical leadership style with ability to develop reusable libraries and automation frameworks to improve efficiency and standardization.
Strong domain knowledge in clinical trials and data review workflows, with practical experience in end-to-end clinical data review programming in regulated environments.