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Senior Medical Director, Clinical Development

Job in New York, New York County, New York, 10261, USA
Listing for: EPM Scientific
Full Time position
Listed on 2026-01-27
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Location: New York

Sr. Medical Director Clinical Development

Northern New Jersey (Hybrid 3x per week on-site)

Compensation: $,000 + Bonus + Equity

An industry-leading biotech with a proprietary discovery platform and a proven leadership team behind one of the most transformative immuno-oncology approvals is looking for a Sr. Medical Director Clinical Development. The company boasts a robust pipeline with multiple late-stage programs and over 10 additional indications, spanning oncology, neurology, and immunology. Backed by top-tier investors and a multi-year cash runway, they are well-positioned for rapid growth and significant impact.

Key Responsibilities
  • Design and lead early‑stage clinical development trials, including assessment of safety and efficacy data, medical monitoring, and other clinical study activities.
  • Collaborate with biomarker, discovery, and translational research teams to integrate scientific insights into clinical development.
  • Interpret study data and reports, and prepare high‑quality written and oral presentations of research findings.
  • Contribute to program‑level strategy discussions within Eikon's therapeutic focus areas.
  • Work closely with Clinical Science, discovery, translational, biomarker research, toxicology, clinical pharmacology, drug safety, regulatory, Global Clinical Operations, and supporting functions to ensure seamless cross‑functional execution.
  • Build strong working relationships with external investigators, key opinion leaders, and alliance partners.
  • Partner with Data Management, Clinical Operations, Biostatistics, and Regulatory to ensure strategic, coordinated, and high‑quality execution of clinical protocols.
  • Collaborate with study physicians and clinical scientists to develop rigorous study protocols and ensure consistent processes and standards across programs.
  • Support responses to protocol‑related questions from health authorities and ethics committees in coordination with functional partners.
Ideal Candidate
  • Medical degree (MD) with fellowship in Oncology.
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Position Requirements
10+ Years work experience
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