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Tier-1 pharma brand, metro location, and mid-level experience increase competition despite niche specimen-management specialization.
Role requires biopharma specimen and lab operations experience, limiting transferability across industries.
Explicit 3-4 years, required biopharma specimen experience and tooling make filtering fairly strict.
Oversee maintenance and quality assurance of the CBI Specimen Management System (SMS) including data cleaning and load file issue resolution.
Manage reference data such as dictionaries and mapping files, support vendor onboarding and data transfer specifications.
Provide analytics and reporting support with advanced custom visualizations, and identify opportunities for process and system improvements.
Bachelor's degree in a scientific or technical discipline; advanced degree is a plus.
3-4 years of experience in biopharma industry focused on clinical drug development.
Exposure to biomarkers, pharmacokinetics, and/or immunogenicity specimen activities; laboratory operations knowledge highly desired.
Data management experience and programming skills; familiarity with analytics tools like Power BI or SpotFire.
Experienced in biopharma clinical development with strong focus on specimen data and laboratory processes.
Comfortable working in a global matrix organization, liaising with diverse internal/external stakeholders to resolve data issues.
Capable of leveraging analytics for complex data problem-solving and driving continuous improvements in specimen data systems.