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Senior clinical-data specialist with domain regulatory requirements limits applicant pool despite Tier-1 brand.
Clinical trial and regulatory specialization makes skills less transferable outside life sciences.
Explicit 8–10 years experience plus CDISC, GCP and clinical database skills enforce strict mandatory filters.
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Develop and maintain Power BI dashboards, reporting tools, and automation solutions to enable independent access to insights and streamline operational workflows.
Lead technical initiatives in Clinical Data Sciences involving automation, BI, and technology, collaborating across multiple stakeholders and functions to align solutions with business objectives.
Create reusable tools and integrations between platforms to improve data flow, reduce duplication, and enhance data quality and confidence across the organization.
Master’s degree in a scientific or healthcare-related field.
8-10 years of experience in clinical data management or a similar role in pharmaceutical or clinical research industry; medical devices experience preferred.
Proficiency in Microsoft Power Suite, automation technologies, and clinical data management software; knowledge of SAS, SQL, and/or Oracle Clinical.
Strong understanding of clinical trial processes, regulatory guidelines (GCP, CDISC), and clinical data management principles.
Experienced in leading technical and automation projects within Clinical Data Sciences with cross-functional collaboration experience.
Skilled in integrating multiple data platforms and building scalable, reusable analytic and reporting solutions.
Familiar with clinical trial design, regulatory standards (FDA/CFR, ICH/GCP), and data privacy regulations (GDPR), facilitating compliant data management and reporting.