GQR | Senior Director Toxicology | boston, ma

3 weeks ago


boston, United States GQR Full time

In This Role, You Will:

  • 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



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