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Director or Senior Director, Program Management

Kymera Therapeutics
August 21, 2026
Full-time
Remote friendly (Watertown, MA)
Worldwide
Clinical Research and Development
Role: Senior Program Manager in biopharma (likely biotherapeutics, given Kymera's focus on targeted protein degradation), responsible for leading cross-functional R&D development teams to achieve program milestones. Responsibilities: manage program planning, risk mitigation, team coordination, stakeholder communication (including executive updates), and governance preparations; establish strategic development plans aligned with asset goals; facilitate team discussions and decision-making; ensure projects stay on timeline and budget; address complex issues proactively. Requirements: 8+ years in biotech/pharma, with at least 4 years in program management; advanced scientific degree (PhD preferred); experience in discovery to clinical development of small molecules; proven leadership in matrix environments; strong communication and influencing skills; proficiency in project management tools like MS Project; PMP certification is a plus. High-Value: experience across preclinical to clinical stages, with a focus on small molecule drug development; strong stakeholder engagement including executive team; ability to coordinate complex cross-functional activities. WorkSetup: not specified, but likely hybrid or onsite given seniority and scope.