Jobs at Kymera Therapeutics

The Executive Director, Talent Acquisition will lead Kymera's talent strategy, manage workforce planning, and enhance candidate experience while building a high-performing team aligned with the company's growth objectives.

Serve as the embedded IT liaison to Clinical, leading requirements gathering, process mapping, and pre-implementation scoping for Veeva Vault QMS/TMF/CTMS. Drive implementations with vendors, support change management and training, ensure GxP and 21 CFR Part 11 compliance, and scope additional clinical technology initiatives (RBQM, portfolio planning).

Lead global commercial strategy, brand planning, and launch readiness for KT-621. Define product vision, positioning, target segments, and value proposition. Drive launch execution, cross-functional alignment, evidence generation, market assessments, and lifecycle expansion across immunology indications. Partner with Clinical Development, Medical Affairs, Market Access, Regulatory, Finance, and Analytics to support successful US and global commercialization.

Lead global and U.S. pricing, reimbursement, access, and value strategies across Kymera's pipeline. Drive payer engagement, pricing governance, evidence-generation alignment with Clinical/HEOR, launch readiness, and lifecycle access optimization. Influence cross-functional strategy, manage market access risks, and support commercial planning to maximize patient access and product value for immunology indications.

Own full-cycle recruiting for late-stage development and commercial roles in a high-growth biotech. Build proactive talent pipelines, partner with hiring managers, provide market intelligence and comp benchmarking, manage candidate activity in Greenhouse, and collaborate with TA team on employer branding and agency management.

Provide strategic and operational leadership for study start-up activities in clinical programs, ensuring compliant site activation and timely execution of trial initiatives.

The Director, Trial Master File will lead TMF platform implementation, oversee compliance, standardize processes, and ensure inspection readiness across clinical operations.

The role involves optimizing proteomics methods, maintaining instruments, analyzing data, and collaborating on drug discovery projects in a fast-paced environment.

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.

The role involves developing and maintaining data workflows for research teams, managing scientific applications and data governance while collaborating with scientists and vendors to deliver scalable informatics solutions.

The Endpoint Systems Engineer will provide advanced support for Windows endpoints, manage security compliance, and handle identity and access management within a hybrid environment, focusing on optimizing user experience and system reliability.

The Associate Director will oversee Quality in GMP activities, ensuring compliance, managing product disposition, and collaborating on regulatory submissions and quality metrics. Key responsibilities include oversight of manufacturing processes and addressing quality issues.

The role involves leading targeted proteomics research, developing and optimizing assays, and collaborating with project teams to inform drug discovery decisions.