The Associate Director or Director of Supply Chain at Kymera will lead the packaging, labeling, and distribution of clinical supplies for various studies, develop supply chain strategies, and manage vendor relationships. They will ensure compliance with regulations and manage import/export processes while coordinating with clinical teams.

The Associate Director, Product Quality will serve as a subject matter expert for GMP activities, overseeing quality aspects of manufacturing and distribution of clinical products, ensuring compliance with regulations, collaborating on technical transfers, and investigating product quality issues. The role involves managing external suppliers and developing quality metrics to track performance.

The Director of R&D Quality oversees compliance for clinical and non-clinical programs, develops strategic quality oversight plans, guides study teams on regulations, implements metrics for continuous improvement, assists in audit processes, and cultivates a culture of quality awareness in line with regulatory standards.

As the Lead Statistician, you will oversee statistical efforts for a clinical program, contribute to the clinical development plan, author statistical sections for regulatory submissions, manage relationships with CROs, and support scientific publications. You will also ensure compliance with global regulatory standards and guide direct reports if applicable.

The Director of IP Counsel at Kymera will manage a complex global patent portfolio, protect innovations from research and clinical projects, conduct strategic portfolio analyses, and provide expert IP counseling to internal teams. The role requires ongoing management of outside counsel and education on IP matters, contributing to patent strategies across the organization.

As a Scientist I in Cellular Pharmacology at Kymera, you will develop and validate immune cell-based assays, design ex-vivo functional assays, and contribute to assay development for inflammatory and metabolic disease targets. Responsibilities include data analysis, pharmacological validation, and maintaining good laboratory records.

The Contracts Specialist/Paralegal will draft, review, and manage various contracts related to biopharmaceutical operations, ensuring compliance with legal standards and internal policies. Responsibilities include overseeing contract lifecycle management, collaborating with cross-functional teams, analyzing contracts, and contributing to process improvements.

The Director of Analytical Development will lead pharmaceutical development projects, focusing on analytical control strategies and methods for small-molecule protein degraders. Responsibilities include collaborating with process chemistry, managing analytical activities with CDMOs, developing test methodologies, and ensuring compliance with regulatory standards.

Lead the talent acquisition function at Kymera, developing innovative recruitment strategies, managing a team, improving talent processes, and fostering trust-based relationships across the company. Champion core values in all recruitment initiatives.