
We are seeking a highly motivated Associate Director to join the Quantitative Pharmacology (QP) group. The Associate Director will lead model-informed drug development strategies supporting one or more therapeutic areas across modalities including antibodies, siRNA, and gene therapies. This role combines scientific depth with cross-functional leadership to inform dose selection, trial design, and regulatory strategy from early development through submission.
A day in the life of an Associate Director may look like:
Driving model-informed development (MIDD) and pharmacometrics strategies in partnership with Clinical Pharmacology, Biostatistics, Clinical and Translational teams to support regulatory and clinical decision-making.
Leading the QP evaluation of one or more assets, accountable for timely delivery of population PK/PD, exposure–response, and translational modeling analyses.
Representing QP at program and governance meetings, communicating quantitative insights clearly to non-modeling audiences.
Contributing to regulatory interactions and authoring key components of regulatory documents related to QP (e.g., IB, briefing books, etc.).
Mentoring and developing junior scientists and fostering a culture of scientific rigor and collaboration.
Identifying and implementing process improvements, new modeling approaches, and innovative quantitative tools to enhance efficiency and impact.
Ensuring analyses and documentation are of the highest scientific quality and regulatory compliance.
This may be the right role for you if you:
Want to make a visible impact on the organization by driving >Salary Range (annually)