Develop the strategy of nonclinical/Toxicology development plans
Propose and implement nonclinical toxicology study design (non-GLP and GLP), and ensure execution of toxicology studies to support company timelines and goals
As a study monitor, direct and oversee nonclinical toxicology studies supporting nonclinical and clinical development programs
Oversee the selection and management of consultants, vendors and CROs
Prepare all nonclinical safety documents to support regulatory filings with global health authorities
Respond to GHA inquiries
Collaborate with cross-functional teams to develop strategies for appropriate data generation in support of candidate nomination, IND filing, and clinical development of new small molecule drug entities
Represent Nonclinical Safety for cross-functional teams