Here at Kelonia Therapeutics, we aren’t just a preclinical company; we’re trailblazers in viral engineering, pushing the boundaries of in vivo lentiviral gene and cell therapy. We're not just a team; we're dreamers on a mission to bring the promise of cell and gene therapy to every patient in need.
At Kelonia, we've gathered a group of pioneers in cell and gene therapy to lead our journey, with extraordinary scientific founders at the helm, providing the cutting-edge technology that sets us apart. We're not just building a company; we're cultivating a culture—one that values both skill and care.
Are you ready to be a part of our remarkable journey? We're looking for someone exceptional to join our growing team as a Principal Scientist in the Preclinical Research group. This isn't just a job; it's an opportunity to contribute to groundbreaking therapies, to be part of a company's inception, and to make a transformative impact on patients' lives. If you're passionate about scaling a company from the ground up, making a real difference, and shaping the inclusive culture we're proud of, this opportunity is tailor-made for you. Join us and be a driving force in achieving excellence in viral engineering.
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Lead the design and validation of cellular and molecular endpoint nonclinical bioassays including those used to understand the mechanism of action
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Manage cross-functional teams and collaborate with external partners to drive projects from conception to regulatory submission.
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Opportunity to manage associates and scientists.
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Collaborate with research and process scientists to execute translational and preclinical safety studies using Kelonia's novel LVV gene delivery technology
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Author and review key documents as required for regulatory submissions
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Implement new technologies and processes to enhance assay performance and maintain industry-leading standard
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PhD in immunology or related field with 4+ years of industry experience (level based on experience)
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Proven ability to work collaboratively, meet deadlines, and balance multiple workstreams
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Excellent communication skills, with the ability to present complex scientific concepts to diverse audiences.
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Experience with cell culture, flow cytometry, ELISA/MSD, IHC, qPCR/PCR/ddPCR
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Experience with ex vivo immune cell sample processing for mouse and NHP studies
- Experience managing contract laboratories and transferring bioassays is a plus
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Strong leadership and project management skills, with a track record of managing complex projects and teams, experience supervising junior scientists preferred.
At Kelonia, we are dedicated to promoting a healthy work-life balance, and our benefits are designed to reflect that commitment. Alongside Flexible Time Off (FTO), we offer a flexible scheduling environment that empowers employees to work in a way that aligns with both their needs and our company’s objectives. We also provide a team-focused environment with a competitive benefits package, including health, dental, commuter benefits, and more. At Kelonia, we foster a collaborative and inclusive workplace where you can join a small team that values both talent development and achieving company goals.
Kelonia Therapeutics is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law. Kelonia does not accept unsolicited resumes from any source other than directly from candidates.
