Insmed Incorporated logo

Senior Director, Clinical Development

Insmed Incorporated
Full-time
Remote friendly (Headquarters, NJ)
United States
$290,000 - $347,600 USD yearly
Clinical Research and Development

Want to see how your resume matches up to this job? A free trial of our JobsAI will help! With over 2,000 biopharma executives loving it, we think you will too! Try it now — JobsAI.

Role Summary

Senior Director, Clinical Development at Insmed. Leads clinical strategy and development activities for mid-to-late-stage programs, focusing on the pulmonary arterial hypertension indication within TPIP. Responsible for clinical input into program strategy, regulatory engagements, and collaboration with cross-functional teams to ensure integrated global plans.

Responsibilities

  • Leads clinical development team responsible for mid-to-late-stage development of TPIP in the PAH indication.
  • Leads the matrix Clinical Study Team (CST) to effectively make decisions and handle conflict and change.
  • Maintains a high degree of CST effectiveness through collaboration, influence, and coaching of cross-functional team members.
  • Collaborates with the Clinical Program Lead to represent the matrix Global Asset Team and ensure the clinical program is integrated into Global plans across functions.
  • Collaborates with the CPL to build strategic and coordinated clinical development plans aligned with business objectives and differentiated from competitors.
  • Responsible for all clinical aspects of the clinical indication strategy.
  • Accountable for the delivery of projects, partnering with other global development and related functions.

Qualifications

  • MD/DO-equivalent with preference for Cardiology or Pulmonary formal training; industry experience in Pulmonary or Cardiology in drug development considered.
  • 6+ years in biotech or pharma with most in a global clinical development role, or equivalent research experience; combination of drug/device experience is a plus.
  • sNDA or sBLA experience or original NDA or BLA experience preferred; J-NDA experience a plus.
  • Experience with FDA advisory committees, CHMP Scientific Advisory Group, or CHMP Oral Explanation preferred.
  • Previous direct people management required.
  • Experience working in matrix development teams (e.g., Global Study Teams) required.

Skills

  • Clinical development leadership
  • Cross-functional collaboration and matrix team governance
  • Regulatory strategy and engagement with health authorities
  • Strategic planning and program management
  • Communication of clinical goals and scientific rationale

Education

  • MD/DO-equivalent; advanced training in Cardiology or Pulmonary preferred
Apply now
Share this job