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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 .
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.
Define and lead the company’s pharmaceutical development strategy across the portfolio, ensuring alignment with corporate priorities and development timelines
Provide strategic leadership for preformulation, biopharmaceutics, and formulation development activities supporting discovery, preclinical, and clinical-stage programs
Champion innovation in formulation sciences and enabling technologies to address complex drug delivery and bioavailability challenges
Drive development and implementation of phase-appropriate drug product development and manufacturing strategies
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Watertown, USA
Watertown, USA
Watertown, USA
Watertown, USA
Watertown, USA
Watertown, USA
Watertown, USA
Watertown, USA
Watertown, USA
Lead a high-performing Pharmaceutical Development team, in internal activities and management of an external network of CROs, CDMOs, and strategic partners
Establish scalable processes, operational frameworks, and best practices to support portfolio growth
Provide strategic oversight of outsourced development and manufacturing activities, ensuring quality, timelines, and technical objectives are achieved
Lead CMC-related regulatory strategy for drug product development activities, regulatory submissions and health authority interactions
Ensure compliance with applicable GMP and regulatory requirements
Represent Pharmaceutical Development in due diligence activities, external collaborations, and interactions with other functions
Contribute to risk assessment, resource prioritization, and investment decisions as a member of the Technical Operations leadership team
Foster strong cross-functional partnerships across Research, Clinical, Regulatory, Quality, Supply Chain, and Program Management to enable efficient advancement of pipeline programs
Clinical-stage biotechnology company developing oral small-molecule degrader medicines for immunological and oncology diseases.
Visit company websiteJobs and hiring trendsUSD 315000-395000 yearly / year
Full-time
Senior · 18+ years experience
Onsite
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