The Medical Director will support clinical development activities for oncology programs, including medical monitoring, safety review, and data analysis. They will also contribute to key clinical deliverables such as study protocols, investigator brochures, and regulatory submission documents.
Requirements summary
Candidates must hold an MD with training in oncology, hematology, or a related field. The role is suitable for early-career professionals, including those transitioning from academia, with a strong interest in cell and gene therapy.
to dramatically expand the benefit and reach of genetic medicines. Our goal is to change what’s possible for genetic medicine by building the capabilities, experience, and commitment to bring life-saving medicine to every patient in need. We are a human-first company, driven by a mission to develop transformative genetic medicines for patients and their loved ones.
We have brought together pioneers in cell and gene therapy, guided by extraordinary scientific founders and a team committed to turning breakthrough science into real-world impact. As we grow, we are building a culture that values rigor, collaboration, and care for one another.
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What You'll Do
Support clinical development activities across 1–2 oncology programs, including supporting our lead clinical program KLN-1010, with the ability to expand scope over time
Perform ongoing medical review of clinical data, including safety, efficacy, and patient-level insights
Contribute to and progressively lead key clinical deliverables, including:
Partner closely with Clinical Operations, Regulatory, Biometrics, and Translational teams to support high-quality study execution
Participate in medical monitoring and safety review activities
Support regulatory submissions and interactions, including preparation of FDA-facing materials, and pharmacovigilance reporting
Engage with investigators and clinical sites to support trial conduct and enrollment
Contribute to clinical strategy discussions, with increasing ownership as experience grow
What You'll Bring
MD required with training in oncology, hematology, or a related field.
Open to candidates directly from academia or with early industry experience (industry experience preferred but not required)
Strong interest in oncology drug development, particularly in cell and gene therapy
Benefits
Health insurance
Flexible scheduling
Commuter benefits
Flexible Time Off
On-site gym
Food hall
Foundational understanding of clinical trial design, safety evaluation, and data interpretation
Interest and willingness to learn and contribute to clinical documentation, including protocols, IBs, and regulatory materials
Ability to analyze clinical data and communicate insights clearly
Collaborative, low-ego mindset with a willingness to be hands-on and learn in a fast-paced environment
The anticipated salary range for candidates for this is below. The final salary offered will depend on several factors, which may include, but is not limited to, relevant years of experience, skills, qualifications, job knowledge, and educational background.
\n $243,000 - $291,000 a year \n
At Kelonia, we’re serious about balance and growth. We offer Flexible Time Off and flexible scheduling aligned with team objectives, a competitive benefits package (health, commuter, and more), and on-site perks including free parking, a state-of-the-art gym, and a food hall, all within a collaborative, inclusive team that invests in your development.
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.
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