Advance the clinical biomarker strategy in oncology and immunology, influencing trial design and patient selection. Lead cross-functional teams to ensure integration of biomarker data, enhancing decision-making and development across multiple programs.

Drive excellence in quality management by leading electronic systems and compliance initiatives, collaborating across diverse teams to enhance processes and continuously improve quality standards in the pharmaceutical sector.

Accelerate progress at the forefront of drug discovery by managing nonclinical safety and toxicology operations, ensuring seamless project execution across functions and disciplines from lead optimization to IND filing.

Play a key role in shaping regulatory strategies for global development programs, ensuring compliance with complex regulatory requirements, and collaborating with cross-functional teams to support marketing applications and product lifecycle management.

Lead end-to-end chemical engineering for drug substance development, ensuring GMP compliance and optimization at CDMOs. Collaborate with cross-functional teams to drive innovation from late-stage development through commercial launch.