Director, Rare Disease R&D & Regulatory Strategy in Cambridge

Director, Rare Disease R&D & Regulatory Strategy in Cambridge

Cambridge Full-Time 85500 - 104500 $ / year (est.) Hybrid
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At a Glance

  • Tasks: Lead late-stage development programmes and drive FDA readiness for rare diseases.
  • Company: Cycle Pharmaceuticals, a pioneering company in rare disease research.
  • Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
  • Other info: Join a dynamic team dedicated to transforming rare disease treatment.
  • Why this job: Make a real difference in patients' lives through innovative R&D strategies.
  • Qualifications: Proven experience in R&D and regulatory strategy in the pharmaceutical industry.

The predicted salary is between 85500 - 104500 $ per year.

Cycle Pharmaceuticals, headquartered in Cambridge, UK, is seeking an accomplished Director of Research & Development.

This full-time role, based in our Cambridge office on a hybrid basis (minimum 3 days in the office), reports to the Chief Strategy Officer.

You will own late-stage development programmes from strategy through execution and regulatory submission, driving FDA readiness and patient impact.

Build and lead a high-performing, cross-functional R&D team across Product Development,

Director, Rare Disease R&D & Regulatory Strategy in Cambridge employer: Cycle Pharmaceuticals

Cycle Pharmaceuticals is dedicated to making a meaningful impact in the field of rare diseases, with a strong focus on oncology, hematology, neurology, and rare metabolic conditions. The company fosters a collaborative work environment that emphasizes professional growth and the importance of every patient. Employees benefit from hybrid working arrangements and the opportunity to contribute to innovative pharmaceutical development.

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Contact Details:

Cycle Pharmaceuticals Recruitment Team

We think you need these skills to ace Director, Rare Disease R&D & Regulatory Strategy in Cambridge

Leadership Skills
Cross-Functional Team Management
Regulatory Strategy
FDA Submission Knowledge
Late-Stage Development Expertise
Project Execution
Strategic Planning