Remote Director, Emerging Therapies Medical Affairs

Insightec

United States

Remote

USD 180,000 - 240,000

Full time

14 days+

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Job summary

Insightec is seeking a Director of Medical Affairs – Emerging Therapies to lead medical innovation and strategy across early- and mid-stage programs leveraging the 220KHz FUS platform. The role focuses on scientific rigor, regulatory readiness, and cross-functional collaboration with R&D, market access, and commercial teams.

The leader will drive external engagement with KOLs and scientific leaders, oversee trials and publications, and guide development plans toward timely commercialization of

Qualifications

  • Experience leading medical affairs for emerging therapies.
  • Strong engagement with KOLs and scientific leaders.
  • Experience in clinical development, regulatory submissions, and market access.

Responsibilities

  • Develop and lead medical strategy for emerging therapies leveraging the 220KHz FUS platform.
  • Collaborate with R&D, regulatory, and commercial to align on portfolio strategy and timelines.
  • Oversee clinical trials readiness and execution, including endpoint definition and data generation.
  • Lead advisory boards and external collaborations with academic partners and KOLs.
  • Drive publications strategy, scientific communications, and podium presence at major congresses.
  • Provide medical input for regulatory submissions and labeling; support safety communications.

Skills

Medical affairs leadership
KOL engagement
Clinical development
Strategic planning
Regulatory & compliance
Cross-functional leadership
Evidence generation

Job description

Insightec is seeking a Director of Medical Affairs – Emerging Therapies to lead medical innovation and strategy across early- and mid-stage programs leveraging the 220KHz FUS platform. The role focuses on scientific rigor, regulatory readiness, and cross-functional collaboration with R&D, market access, and commercial teams.

The leader will drive external engagement with KOLs and scientific leaders, oversee trials and publications, and guide development plans toward timely commercialization of

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