Medical Director, Clinical Development

Role Overview

• Support clinical development activities across 1–2 oncology programs, including supporting our lead clinical program KLN-1010
• Perform ongoing medical review of clinical data, including safety, efficacy, and patient-level insights
• Contribute to and progressively lead key clinical deliverables, including:
• Clinical study protocols and amendments
• Investigator’s Brochures
• Clinical study reports and medical summaries
• Regulatory submission documents (e.g., INDs, briefing materials)
• 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 grows

Requirements

• 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
• 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

Benefits

• Flexible Time Off
• Competitive benefits package (health, commuter, and more)
• On-site perks including free parking, a state-of-the-art gym, and a food hall