The Vice President, Program Management oversees Kymera's Program Management Office, ensuring program strategies are optimized and effectively organized for decision-making. Responsibilities include leading program management support, resource allocation, fostering high-performance teams, and driving major scaling initiatives in drug development and commercialization.

The Associate Director, GCP Quality ensures compliance with GCP across clinical trials, providing quality oversight, risk management, and training.

Lead development of machine learning models for drug discovery, integrating ML with molecular modeling to enhance molecular design and optimization approaches.

The Director/Sr. Director, DMPK will set strategy and drive execution for drug metabolism and pharmacokinetics in drug development, collaborating with multifunctional teams and managing CRO interactions.

Lead statistical efforts in clinical programs, ensuring compliance with regulations, contributing to clinical protocols, and managing CRO relationships. Oversee statistical outputs and guide team members.

Develop, optimize, and implement targeted proteomics workflows, manage activities at CROs, perform mass spectrometry assays, and analyze data to support drug discovery.

The Senior Manager/Associate Director of Supply Chain will manage supply planning and execution for clinical studies, ensuring timely supply of materials and compliance with regulations while collaborating on strategy and risk management.