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Medical Director, Clinical Development
Kelonia TherapeuticsMedical Director focused on clinical development for groundbreaking genetic medicines. Collaborating with teams to support oncology programs and contribute to transformative therapies.
Posted 5/5/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesLead💰 $243,000 - $291,000 per yearWebsite
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Comp & perks- 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
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial designsafety evaluationdata interpretationclinical study protocolsinvestigator’s brochuresclinical study reportsregulatory submission documentspharmacovigilance reportingmedical monitoringoncology drug development
Soft Skills
collaborative mindsetcommunication skillsanalytical skillswillingness to learnhands-on approachlow-ego mindsetability to engage with investigatorsability to support trial conductability to contribute to discussionsadaptability in fast-paced environment
Certifications
MD