Senior Director of In Vivo Pharmacology

3 days ago

South San Francisco, California, United States Meet Full time
Job Summary

We are seeking a highly experienced Senior Director to lead our In Vivo Pharmacology team. As a key member of our Research organization, you will be responsible for designing, implementing, and overseeing in vivo pharmacology studies to support our gene therapy programs.

Key Responsibilities
  • Provide strategic leadership and direction to the In Vivo Pharmacology team, ensuring the successful execution of studies and the delivery of high-quality data.
  • Collaborate with cross-functional teams, including Research, Development, and Regulatory, to ensure alignment and effective communication.
  • Develop and implement innovative research strategies and plans to support our gene therapy portfolio.
  • Manage and oversee the design, implementation, and conduct of in vivo pharmacology studies, including the identification and selection of suitable contract research organizations (CROs).
  • Investigate and initiate innovative approaches to identify appropriate pre-clinical and clinical biomarkers.
  • Foster effective collaboration and communication with internal teams, external partners, and key stakeholders to ensure alignment of research objectives and facilitate knowledge sharing.
  • Develop and present Pharmacology strategy, plans, and data at project team meetings and to management to support project objectives.
  • Support the filing of regulatory documents, including preparation of final study reports and IND (or related) documents.
Requirements
  • MD/PhD in Molecular & Cell Biology, Genetics, Biochemistry, Immunology, Physiology, or related areas.
  • Minimum 15 years of experience designing, executing, and overseeing in vivo pharmacology studies to support projects in the pharmaceutical or biotech industry.
  • Previous experience managing in vivo pharmacology studies in an industry setting, with experience in overseeing non-GLP and GLP studies is required.
  • Minimum 10 years of experience managing teams and cross-functional projects, preferably in the gene therapy field.
  • Experience in generating and managing pre-IND reports is strongly preferred.
  • Prior experience with gene therapy platforms is strongly preferred.
  • Previous experience working in fast-paced start-up environments preferred.
Benefits

We offer a comprehensive benefits package, including equity and ownership in a fast-growing company, access to a 24-hour gym, comprehensive medical, dental, and vision, commuting stipend based on your geographical location, 401(k) match, and flexible time off policy.

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