Position Description:Calico is seeking a Principal Scientist, Drug Metabolism and Pharmacokinetics to join our Drug Discovery team. This position is a unique opportunity to shape the DMPK strategy and contribute to the development of innovative therapeutics. This role will function as an individual contributor, collaborating closely with external partners such as Pharma and CROs.
Position Responsibilities: Strategic Leadership
- Develop and implement the DMPK strategy to support drug discovery and development programs
- Provide expert DMPK guidance and input to project teams
- Represent the DMPK function in cross-functional meetings and interactions with external stakeholders
- Stay abreast of the latest advancements in DMPK science and regulatory guidelines
- Collaborate closely with project, biology, and chemistry leads to support and advance programmatic goals
Collaboration and Outsourcing
- Effectively collaborate with CROs and other external partners to execute DMPK studies
- Manage CRO relationships, including study design, data analysis, and report writing
- Oversee the quality and timely delivery of DMPK data from external partners
Individual Contribution
- Design, coordinate and interpret DMPK studies, including in vitro and in vivo experiments
- Analyze and interpret DMPK data to support drug candidate selection and development
- Author and review DMPK reports, regulatory documents, and scientific publications
Position Requirements: - Ph.D. in pharmacokinetics, drug metabolism, or a related field
- 8+ years of experience in DMPK within the pharmaceutical or biotechnology industry
- Experience as a DMPK functional representative on drug discovery teams
- Strong understanding of DMPK principles and their application to drug discovery and development
- Extensive experience in designing and conducting in vitro and in vivo DMPK studies
- Proven ability to analyze and interpret DMPK data to inform drug development decisions
- Excellent communication, interpersonal, and collaboration skills
- Experience in managing CROs and external partnerships
- Must be willing to work onsite 5 days a week
Nice To Have: - Experience with a variety of therapeutic modalities, including small molecules, biologics, and peptides
- Familiarity with regulatory guidelines and requirements for DMPK studies
- Prior experience in writing regulatory documents is highly desirable
- Experience with modeling and simulation software such as Phoenix WinNonlin, Gastroplus, SimCYP
The estimated base salary range for this role is $197,000 - $235,000. Actual pay will be based on a number of factors including experience and qualifications. This position is also eligible for two annual cash bonuses.
