The Director of Process Engineering at Kymera leads the development and optimization of small-molecule drug manufacturing processes, ensuring compliance with regulatory requirements while driving operational excellence and cross-functional collaboration.

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.

Lead statistical programming efforts for clinical studies, ensuring compliance and quality deliverables, while collaborating with teams and managing vendor relationships.

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

The intern will assist in statistical analysis of clinical trial data, support development of statistical plans, and perform exploratory data analysis in a pharmaceutical setting.

The intern will assist the business development team with market research, competitive analysis, due diligence, and collaborative projects, enhancing skills in biopharmaceutical strategy.

The Desktop Engineer will provide advanced support for endpoint devices, ensuring security and reliability in a hybrid MS environment, while collaborating across teams and managing user identity and access.

The Site Engagement Lead fosters partnerships with clinical trial sites, executing engagement strategies, supporting recruitment, and collaborating with cross-functional teams to enhance trial success.