Description

You will design and execute clinical biomarker strategies to support early response monitoring, patient stratification, and understanding resistance mechanisms in oncology clinical trials. You will collaborate with internal teams and CROs to oversee biomarker assay development, qualification, and sample analysis, and analyze biomarker data in the context of clinical outcomes.

Requirements

• PhD in relevant scientific discipline with 3+ years industry experience in clinical biomarkers or translational medicine
• Experience supporting oncology clinical trials with biomarker components
• Familiarity with biomarker platforms such as genomic/molecular and proteomic assays
• Experience working with CROs and managing external vendors
• Strong scientific communication skills and ability to work cross-functionally

Responsibilities

• Design and execute clinical biomarker strategies for early response monitoring, patient stratification, and resistance mechanisms
• Support biomarker implementation in early- and late-stage oncology clinical trials
• Oversee biomarker assay development, qualification, and sample analysis with internal teams and external CROs
• Analyze and interpret biomarker data in context of clinical outcomes and present results cross-functionally
• Contribute to clinical protocols, study reports, and regulatory documents (INDs, IBs, CSRs)