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Senior Medical Director, Clinical Development

Amylyx Pharmaceuticals
Full-time
Remote friendly (United States)
United States
$311,000 - $350,000 USD yearly
Clinical Research and Development

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Role Summary

Senior Medical Director, Clinical Development

Amylyx is seeking a Senior Medical Director, Clinical Development to lead a late-stage, pivotal program and potentially expand to additional programs with the same molecule. The role includes medical monitoring, development and execution of the Clinical Development Plan, collaboration with multidisciplinary teams, and interaction with internal and external stakeholders. Opportunities to lead additional development programs and manage a small team of clinical scientists and physicians may arise.

Responsibilities

  • Provides medical monitoring to assigned clinical trials in the arenas of serious endocrine conditions, neurodegenerative and/or rare disease
  • Provides clinical development leadership for programs that integrate extensive knowledge in clinical science with inputs from the global medical and patient communities
  • Works closely with Medical Directors, Pharmacology, Drug Discovery, external experts, and investigators to accumulate scientific and medical knowledge necessary to support clinical development plans
  • Integrates scientific rationale, regulatory requirements, product development plan, and value to patients and shareholders to build a solid Clinical Development Plan (CDP)
  • Accountable for production of highest quality program related documents, including protocols, IBs, clinical study reports, briefing documents and drug labels
  • Develops and maintains relationships with program counterparts in Research, Regulatory Affairs, Clinical Operations, Statistics and Contract Research Organizations (CROs)
  • Acts as the primary Clinical Development interface with internal stake holders as well as external subject matter experts and alliance partners for the assigned programs
  • Contributes to specific Business Development activities and various organizational initiatives in Clinical Development

Qualifications

  • MD required
  • Experience with late-stage clinical development and drug development in rare diseases strongly preferred
  • 4+ years of experience in leading clinical development programs in the biotechnology/pharmaceutical industry with a proven record of achievements
  • Ability to think critically and demonstrate troubleshooting and problem-solving skills
  • Demonstrated leadership and team building skills as well as the ability to perform effectively in a multi-disciplinary environment
  • Ability to lead directly and by influence, including strong interpersonal, problem solving, conflict resolution and analytical skills in a matrix environment
  • Excellent communication skills (oral and written) and organizational skills
  • Ability to travel internationally and domestically

Skills

  • Medical monitoring
  • Clinical development planning
  • Regulatory understanding
  • Cross-functional collaboration
  • Data review and interpretation
  • Leadership and team management

Education

  • MD required

Additional Requirements

  • Ability to travel internationally and domestically
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