CellCarta
The Clinical Study Specialist I will support the operational success and integrity of oncology clinical trials by managing site-level regulatory documentation, monitoring visits, and action item follow‑up. Acting as a liaison between Project Management, Regulatory Affairs, and Quality Assurance, the role ensures precise execution of site initiation, monitoring, and close‑out activities across a portfolio of complex studies.
CellCarta is a global contract research organization that provides precision medicine testing services to biopharma and research organizations. Their laboratory offerings include immunology, histopathology, proteomics, genomics and digital pathology to support biomarker development, translational research and clinical trial testing. CellCarta pairs customizable assays, advanced imaging and data analysis with regulatory-minded workflows to accelerate development and decision-making.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
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and employee contacts for CellCarta.
14% below the average for this role