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Tier-1 brand and metro location increase competition, niche clinical/Veeva skills moderately limit applicant pool.
Requires clinical trial processes and Veeva-specific experience, limiting transferability across industries.
Regulated clinical domain with mandatory Veeva, R/Python, SQL and reconciliation expertise enforces strict filters.
Design, develop, validate, and maintain complex clinical data review solutions and reporting tools.
Lead implementation of clinical data review workflows including CDB Checks, Listings, Reconciliations, Medical/Safety Reviews, PD Reviews, and CDMS reporting.
Provide technical oversight for solution architecture, coding standards, validation, and quality compliance; mentor programmers and collaborate with Data Management and cross-functional teams.
Advanced experience in Clinical Data Management, Clinical Data Review Programming, or related clinical systems roles.
Strong expertise in Veeva CDB, Veeva CDMS Reports, Domino, R, Python, SQL, and clinical data standards.
Deep understanding of clinical trial processes, data review methodologies, reconciliations, and regulatory requirements.
Work Experience Required: Not explicitly mentioned in the JD.
Able to lead complex technical initiatives and influence cross-functional stakeholders in clinical data review.
Experienced in designing scalable, automated clinical data workflows and visualizations supporting study milestones and inspection readiness.
Technically proficient with data reconciliation across multiple clinical data sources and skilled in mentoring technical teams.