Senior Clinical Scientist

Alkeus Pharmaceuticals Inc

Cambridge, MA, United States
Base: $160k - $240k; bonus/equity: 15%-20% discret...
On-site
Phase 3 clinical trials
Rare disease ophthalmology
Clinical development strategy
The Senior Clinical Scientist will provide scientific leadership and oversight for late-stage (Phase 3) clinical development programs in rare disease ophthalmology, ensuring scientific integrity and regulatory readiness

Job Summary

  • The Senior Clinical Scientist will provide scientific leadership and oversight for late-stage (Phase 3) clinical development programs in rare disease ophthalmology, ensuring scientific integrity and regulatory readiness.
  • This role involves leading or co-leading the development of pivotal study protocols, serving as the scientific point of contact, and collaborating with cross-functional teams including clinical operations, biostatistics, and regulatory affairs.
  • Compensation includes a base salary range of $160K - $240K, a discretionary bonus of 15%-20%, incentive stock options, and comprehensive benefits.

Matching Summary

The Senior Clinical Scientist will provide scientific leadership and oversight for late-stage (Phase 3) clinical development programs in rare disease ophthalmology, ensuring scientific integrity and regulatory readiness.

Salary

Base: $160K - $240K; Bonus/Equity: 15%-20% discretionary bonus, initial grant of incentive stock options; Benefits: group medical/dental/vision, disability, life insurance, 401(K), flexible time off

Skills & Requirements

Must-have

  • Phase 3 clinical trials
  • Rare disease ophthalmology
  • Clinical development strategy
  • Regulatory document preparation
  • Scientific data interpretation

Nice-to-have

  • Entrepreneurial mindset
  • Fast-paced environment
  • Collaborative leadership style
  • Proactive approach

Key Requirements

  • Master's or Ph.D. in a relevant scientific discipline
  • 6-10+ years of experience in clinical development
  • Demonstrated experience supporting Phase 3 clinical trials
  • Experience in rare disease and/or ophthalmology drug development
  • Experience supporting regulatory interactions and submissions

Work Rights

Not specified

Tailored Resume

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