As a Scientist I at Kymera, you will conduct laboratory experiments, maintain equipment, handle lab inventory, and support cross-functional teams in pharmaceutical compound synthesis.

Develop and implement translational models to guide therapeutics for clinical success, collaborating across functions to optimize drug candidates and support IND submissions.

The Associate Director will lead statistical programming for clinical studies, ensuring compliance, high-quality deliverables, and effective collaboration with internal teams and vendors.

The Senior Manager, Trial Optimization Lead is responsible for developing patient recruitment and retention strategies, overseeing trial efforts, and collaborating with sites to enhance enrollment and engagement in clinical trials.

The Vice President of Safety and Pharmacovigilance will oversee global pharmacovigilance activities, ensure compliance with regulations, and provide strategic safety leadership across clinical programs.