Associate Director, PKPD Modeling
Summary: The Associate Director role can be based in Cambridge, San Francisco, or Princeton in a hybrid capacity. You will be responsible for developing and executing Model Informed Drug Development plans and strategies from the early translational to the late-stage clinical development. You will oversee and report modeling and simulation projects within the company, as well as participate in the strengthening of internal Pharmacometrics.
Key Responsibilities:
- Oversee and report modeling & simulation projects
- Develop and execute MIDD strategies/plans
- Apply Model Informed Drug Development methodologies to contribute to decision making with partner functions (e.g. clinical pharmacology, biostatistics, clinical development)
- Strengthen and build internal PMX platform capabilities (e.g. disease progression modeling, clinical trial simulations, model based meta-analysis)
Key Qualifications:
- Experience in R, NONMEN and/or MONOLIX, SimCYP and related pharmacometrics software
- Strong interpersonal skills cultivating a network of productive relationships
- Demonstrated ability for productive collaboration and ability to adapt to changing business needs
- General knowledge of oncology, immune-oncology, and/or immunology
