Senior Clinical Development Director

Ipsen Biopharmaceuticals Inc.

Cambridge, MA, USA
Base: $255,000 - $306,000; bonus/equity: eligible ...
Fully remote
5+ years clinical research experience
Design and conduct phase i-iii trials
Medical expertise in rare liver diseases
Ipsen Biopharmaceuticals Inc. is seeking a Senior Clinical Development Director to lead clinical programs in rare liver diseases within their Rare Diseases Therapeutic Area. The role emphasizes medical guidance in clinical trials and requires significant experience in drug development

Job Summary

  • The role involves providing medical guidance and leadership in the design and implementation of clinical development programs for rare liver diseases.
  • Candidates must possess an advanced scientific degree such as MD, PhD, or PharmD along with significant industry experience.
  • Ipsen offers a comprehensive benefits package including 401(k) contributions, parental leave, and flexible spending accounts.

Matching Summary

Match Score: 85

Ipsen Biopharmaceuticals Inc. is seeking a Senior Clinical Development Director to lead clinical programs in rare liver diseases within their Rare Diseases Therapeutic Area. The role emphasizes medical guidance in clinical trials and requires significant experience in drug development.

Salary

Base: $255,000 - $306,000; Bonus/Equity: Eligible for short-term incentives; Benefits: Comprehensive package including 401(k), medical, dental, vision, life insurance, and parental leave

Skills & Requirements

Must-have

  • 5+ years clinical research experience
  • Design and conduct Phase I-III trials
  • Medical expertise in rare liver diseases
  • Regulatory submission knowledge IND/CTA/NDA/MAA
  • ICH GCP adherence and patient safety

Nice-to-have

  • Pediatric hepatology expertise preferred
  • Experience with CRO collaboration
  • Strong cross-functional leadership skills
  • Ability to thrive in fast-paced environment

Key Requirements

  • Advanced scientific degree (MD, PhD, or PharmD)
  • 5+ years pharmaceutical or CRO experience
  • Experience with regulatory submissions (IND/CTA/NDA/MAA)

Work Rights

Not specified

Tailored Resume

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