Kymera Therapeutics
Director, Study Start-Up
Watertown, MA · Director
Sponsorship not specified$195k-$275kDetected 67 days ago
GCPComplianceProject ManagementProcess ImprovementClinical TrialsClinical ResearchResearchExperimental DesignLeadershipCommunicationProblem Solving
About the role
- Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics.
- For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn.
- 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.
Skills
- 10+ years of experience in the biotech/pharmaceutical industry with direct experience in project management within Clinical Operations
- Proven track record in process improvement, clinical trial execution, and operational strategy.
- Experience with planning, management, and oversight of activities and deliverables within Clinical Operations
- Strong understanding of clinical trial management, ICH-GCP, and regulatory compliance
- Proven track record of managing multiple projects and/or programs concurrently
- Excellent analytical, problem-solving, and organizational skills.
- Strong communication and interpersonal skills with the ability to influence cross-functional stakeholders.
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 - $275,000, 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.
Company info
- 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.
- 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.
- 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.
- BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.
- How you'll contribute:
- Provide strategic and operational leadership for end‑to‑end study start‑up activities across assigned clinical programs, ensuring timely, compliant, and high‑quality site activation.
- Accountable for development, execution, and ongoing optimization of study‑specific start‑up strategies, including country selection, regulatory and ethics submissions, site feasibility and selection, contract and budget execution, and site activation readiness.
- Establish and maintain clear start‑up timelines, metrics, and dashboards; proactively identify risks to activation timelines and drive mitigation plans to achieve first‑patient‑in (FPI) and enrollment targets.
Equal opportunity
- 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.
Visa & Work Authorization
- veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class
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This listing is sourced directly from Kymera Therapeutics's careers page and normalized into a canonical job model.