Executive Medical Director

3 days ago


San Diego, California, United States Meet Full time
Job Title: Executive Medical Director

Location: Flexible (Remote, Hybrid, or Onsite)

Company Overview:

Meet is partnering with a leading biotechnology company at the forefront of genetic medicine, dedicated to transforming the treatment landscape for patients with rare and neurologic diseases.

Position Overview:

This position is instrumental in shaping and executing development strategies for our neurology portfolio, focusing on neuromuscular diseases.

Key Responsibilities:

  • Lead and oversee multiple Clinical Project Teams, driving the design and implementation of Development Plans for Phase 3 programs in neurology.
  • Play a key role in building and leading a team to advance a neuromuscular disease asset, leveraging leading-edge technology in this therapeutic area.
  • Collaborate with external medical/scientific advisors, thought leaders, and clinical investigators, while engaging closely with internal stakeholders across Research, Development, and Commercial teams.
  • Contribute to Integrated Development Plans, ensuring alignment with strategic vision and regulatory requirements. Proactively address clinical development pathway gaps such as biomarker and natural history study needs.
  • Engage with regulatory agencies to design and develop efficient clinical programs, leveraging novel trial designs and regulatory mechanisms.

Requirements:

  • MD with approximately 5 years of industry experience, demonstrating strong leadership in clinical development across early- to late-stage therapeutic programs.
  • Proven track record in rare neurologic and/or neuromuscular diseases preferred, with experience in leading clinical development efforts in both large and small biopharmaceutical companies.
  • Expertise in clinical trial design, including adaptive designs, and comprehensive understanding of preclinical and clinical development processes.
  • Successful history of developing, planning, and executing clinical studies leading to therapeutic registrations.
  • Experience with regulatory submissions and interactions, including novel trial designs and indications.


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