Senior Medical Director, Clinical Development


Jersey City
USD280000 - USD330000
PR/575795_1768602026
Senior Medical Director, Clinical Development

Sr. Medical Director Clinical Development

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

Compensation: $280,000-330,000 + 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 earlystage 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 highquality written and oral presentations of research findings.
  • Contribute to programlevel 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 crossfunctional 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 highquality 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 protocolrelated questions from health authorities and ethics committees in coordination with functional partners.

Ideal Candidate

  • Medical degree (MD) with fellowship in Oncology.
  • 3+ years in industry.