Director, Preclinical Development
- Employer
- BigHat Biosciences
- Location
- San Mateo, CA
- Start date
- Jul 23, 2022
View more
- Discipline
- Clinical, Clinical Development, Clinical Medicine, Medical Affairs
- Required Education
- Doctorate/PHD/MD
- Position Type
- Full time
- Hotbed
- Biotech Bay
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The Role: BigHat Biosciences is seeking an exceptional individual to lead next-generation antibody development for BigHat’s therapeutic programs.
This role reports directly to the CSO; works closely with other executives and senior leaders; and has broad responsibilities across BigHat for pipeline development.
Key Responsibilities The goals and responsibilities of this position include:
About You
This role reports directly to the CSO; works closely with other executives and senior leaders; and has broad responsibilities across BigHat for pipeline development.
Key Responsibilities The goals and responsibilities of this position include:
- Lead the progression of molecules from lead to therapeutic candidate nomination through PK, PD, and toxicological assessment in relevant animal models
- Source, evaluate, and develop the key assays for advancing lead molecules, including identification and management of relationships with CROs where appropriate
- Contribute to designing TPP and other internal program development activities as part of the Therapeutic Programs Team
- Collaborate across BigHat to ensure our platform capabilities enable the preclinical development of state-of-the-art biologics uniquely possible on BigHat’s platform
About You
- A dynamic thinker with a 5+ year track record of leading key aspects of development programs at a top-tier drug development company along with a deep understanding of the underlying science (MD or PhD).
- Experience with all aspects of antibody development starting after target validation and early hit evaluation through all aspects of preclinical development; experience fulfilling requirements of regulatory filings to initial clinical testing is desired but not essential
- Able to manage multiple unrelated projects concurrently including relationships with collaborators, partners, or CROs to advance a lead molecule to regulatory submission in a timely manner.
- A get-it-done mentality; experience operating in lean organizational structures.
- Superb execution and communication skills
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