The Manager, Auditor is responsible for executing the global Quality Assurance program audits related to GCP compliance. This includes conducting audits of clinical trial sites, evaluating processes, and ensuring compliance with regulations and SOPs. The role requires critical thinking to assess risks and provide strategic audit approaches.

The Director of Molecular Pathology will guide R&D and clinical trial projects, oversee NGS technology implementation, conduct pathology reviews, collaborate with teams, and ensure compliance in a CLIA laboratory setting. Responsibilities include biomarker strategy support, quality control of pathology data, and providing expertise in various molecular technologies.