Lead the evaluation and medical review of safety data across clinical trials, ensuring patient safety and regulatory compliance while guiding cross-functional collaboration and quality assurance in pharmacovigilance operations.

Help us shape the future of Companion Diagnostics by leading global strategies for precision medicine. Drive cross-functional collaboration and bring your expertise in oncology biomarkers to support the development of innovative therapies.

Lead the charge in ensuring robust global patient safety processes while mentoring a high-performing team. Innovate within pharmacovigilance activities, driving compliance and strategic direction in a dynamic regulatory landscape.

Champion biostatistical excellence in late-stage oncology studies, leading cross-functional teams to ensure scientific rigor, timely deliverables, and strategic insights that inform program-level decision-making and regulatory interactions.

Contribute to the design and execution of innovative clinical biomarker strategies for oncology trials. Collaborate with cross-functional teams to validate assays and manage CRO relationships, ensuring successful development from phase 1 to phase 3 studies.