Jobs at Kymera Therapeutics

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.

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 Kymera's business development strategy by sourcing, evaluating, negotiating, and closing collaborations and licensing deals. Manage transactions end-to-end, coordinate cross-functional diligence, prepare partnering materials and financial analyses (NPV, forecasts, comparables), negotiate agreements, and represent the company at industry events to build strategic partnerships.

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

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

Serve as scientific and operational lead for outsourced GLP and non-GLP toxicology studies, liaising with CROs, reviewing protocols and data, monitoring study conduct and quality, managing timelines and risks, reviewing reports, maintaining audit-ready study documentation, and representing Preclinical Safety on cross-functional teams.

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.

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 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.

Lead Kymera's enterprise AI strategy and roadmap; prototype, build, and deploy AI/LLM solutions; select and govern AI platforms; establish AI governance with InfoSec; manage vendors and external engagements; drive adoption through training; and advise functional leaders to operationalize AI across research, development, regulatory, and G&A.

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

Lead strategic sourcing for R&D vendors (CROs, CMOs), manage supplier relationships, negotiate MSAs/SOWs, run RFPs and vendor selection, identify cost savings, track contract status and vendor performance, and improve sourcing processes across the organization.