Contract research organization providing clinical development and regulatory services
Zenith LifeScience is a CRO focused on clinical data management, drug safety, regulatory affairs, and quality assurance for pharma clients. The tech stack—SAS, JMP, Benchling, LC-MS, CDISC, and document management via SharePoint—reflects a lab and compliance-heavy operation. Active hiring is concentrated in research roles with mid-to-senior seniority, and current projects span SDTM dataset work, small-molecule discovery, AAV vector production, and CTMS tool implementation, suggesting expansion into new therapeutic modalities and digital infrastructure.
Zenith LifeScience is a Contract Research Organization and staffing firm serving pharmaceutical and healthcare companies across clinical development and lifecycle management. The company operates out of South Plainfield, New Jersey, with 51–200 employees. Core service lines include clinical trial execution, drug safety (pharmacovigilance), clinical data management, regulatory affairs, quality assurance, and healthcare IT. The business model combines permanent consulting staff placement with project-based CRO delivery, positioning them as both a staffing and services provider to life-sciences companies navigating drug development workflows.
Primary tools include SAS, JMP, Benchling, LC-MS, CDISC standards, ReadSoft, SharePoint, and Concur. Equipment: ddPCR. Used for clinical data management, regulatory compliance, lab workflows, and document control.
Current projects include SDTM dataset development, oncology target validation, small-molecule drug discovery, AAV vector production and purification, CTMS tool setup, digital image analysis implementation, and study document archiving and compliance.
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