Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn.
How we work:
- PIONEER: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.
- COLLABORATE: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.
- BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.
How you’ll make an impact:
- Provides program management and matrixed leadership to cross functional R&D Development teams to drive development and deliver results to meet corporate objectives/goals.
- Predicting and planning solutions to achieve program goals
- Drive clarity and remove barriers to ensure team success
- Interface with management and influence informed decision making
- Proactive management and mitigation of development risks
- Ensure appropriate communication and interface with governance
- In partnership with Program Team Lead (PTL), establish and obtain alignment on asset strategies and integrated development plans.
- Establish, coordinate and facilitate effective team discussions at cross-functional program team meetings. establish meeting agendas, driving clear and timely actions, scenarios planning, driving decisions and holding team members accountable. Identify and manage any additional subteams necessary to develop, maintain and execute strategy/integrated development plans
- Ensure successful execution to timeline and budget of all development activities while proactively identifying key risks and mitigations. Independently resolve complex issues and competing priorities that may impact achievement of goals, creates mitigation plans and drive resolution
- Proactively manage key company stakeholders (executive leadership team): clearly and concisely communicate internal program issues, formulate a position/strategy, and participate and/or drive the resolution process.
- Manage scheduled and ad hoc program reporting; Responsible for coordinating preparation for governance to support and drive asset objectives and deliverables.
- Play a key role in ensuring team effectiveness; health checks and action plans to boost team productivity.
- Support project management and corporate initiatives as needed.
Skills and experience you’ll bring:
- 8+ years in biotech or pharmaceutical environments with a minimum of 4 years in program management
- PhD or other advanced degree in scientifically oriented discipline preferred; PMP certification is a plus
- Track record of having managed internal programs, as well as a desire and ability to perform at a strategic leadership level as well as in a hands-on capacity
- Discovery, Research and Drug Development experience: pre-clinical discovery programs through all stages of small molecule drug development through registration and life cycle management.
- Proven success as a cross-functional leader in managing matrix teams in highly complex, fast-paced environment
- Excellent interpersonal, oral, and written communication skills, including specifically, the skills needed to manage difficult conversations and interactions as they arise
- Strong influential skills and able earn the trust and respect of internal stakeholders while driving initiatives forward
- Project Management Expertise/Organizational Skills
- Scientific Knowledge
- Business Acumen
- Highly proficient in Microsoft Project (or similar), visualization tools including PowerPoint, and other planning/tracking software/platforms.
Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.
Compensation
- Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.
- The anticipated base salary range for this role is $195,000 – $330,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.
- Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.
Skills Required
- 8+ years of experience in biotech or pharmaceutical environments
- At least 4 years of program management experience
- PhD or other advanced degree in a scientifically oriented discipline
- Experience managing internal programs
- Discovery, research, and drug development experience spanning preclinical discovery through registration and lifecycle management
- Proven success leading cross-functional matrix teams in complex, fast-paced environments
- Excellent interpersonal, oral, and written communication skills
- Ability to manage difficult conversations and interactions
- Strong influencing skills and ability to earn stakeholder trust and respect
- Project management expertise and organizational skills
- Scientific knowledge
- Business acumen
- High proficiency in Microsoft Project or similar tools, PowerPoint, visualization tools, and planning/tracking software
- PMP certification
Kymera Therapeutics Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Kymera Therapeutics and has not been reviewed or approved by Kymera Therapeutics.
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Fair & Transparent Compensation — Pay is considered market‑competitive for core scientific and leadership roles, with clearly posted ranges visible for U.S. openings. Feedback suggests strong base pay aligns with comments about high salary and good pay.
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Equity Value & Accessibility — Employees are eligible to participate in broad‑based equity programs, including an equity incentive plan and an ESPP. Feedback suggests this ownership opportunity can meaningfully augment total compensation in a growth‑focused setting.
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Leave & Time Off Breadth — Company‑wide office shutdowns, standard PTO, and summer schedules are promoted to help people unplug. Feedback suggests these practices contribute to a well‑rounded time‑off offering.
Kymera Therapeutics Insights
What We Do
Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on delivering oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Kymera is also progressing degrader oncology programs that target undrugged or poorly drugged proteins to create new ways to fight cancer. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years






