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Tier-1 employer and metro location increase competition, but niche clinical tools moderate applicant density.
Clinical trial systems and Veeva/CDMS expertise make cross-industry transferability low.
Role requires domain-specific tools (Veeva, CDMS) and clinical reconciliation expertise, enforcing moderate screening filters.
Design, develop, validate, and maintain complex clinical data acquisition and review solutions including CDB Checks, Listings, Reconciliations, Medical/Safety Reviews, PD Reviews, and CDMS reporting.
Provide technical leadership on solution architecture, coding standards, validation, and compliance ensuring high quality, inspection-ready clinical data outputs.
Collaborate cross-functionally and mentor programming teams to deliver scalable automated workflows and continuous improvement in clinical data review processes.
Advanced experience in Clinical Data Management or Clinical Data Review Programming roles.
Strong expertise with Veeva CDB, Veeva CDMS Reports, Domino, R, Python, SQL, and 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.
Proven ability to lead complex technical initiatives and influence cross-functional stakeholders in clinical data review.
Experienced in developing reusable libraries and automation capabilities to improve efficiency and standardization in clinical data management.
Comfortable working with diverse clinical data sources (EDC, laboratory, safety, imaging) and driving innovation within established clinical trial environments.