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Tier-1 employer, metro location, and mid-level specialized clinical-data role yields moderate competition.
Clinical trials and Veeva/CDMS focus creates high domain specificity and limited cross-industry transferability.
Requires specialized clinical-data, Veeva/CDMS, regulatory and reconciliation expertise, making screening stringent.
Design, build, validate, and maintain clinical data acquisition and review solutions, including CDB Checks, Listings, Reconciliations, and CDMS reporting.
Lead technical oversight and implementation of complex clinical data workflows and reporting assets ensuring quality, compliance, and scalability.
Mentor programming teams and collaborate with Data Management and cross-functional stakeholders to meet study milestones and deliver inspection-ready outputs.
Advanced experience in Clinical Data Management, Clinical Data Review Programming, or related clinical systems roles.
Technical proficiency in Veeva CDB, Veeva CDMS Reports, Domino, R, Python, SQL, and clinical data standards.
Deep understanding of clinical trial processes, data review methodologies, and regulatory requirements.
Work Experience Required: Not explicitly mentioned in the JD.
Experienced in leading complex clinical data technical initiatives with ability to influence cross-functional teams.
Strong background in designing automated, scalable clinical data review workflows and reporting solutions.
Knowledgeable in reconciliation across diverse clinical data sources (EDC, laboratory, safety, imaging).