Director, Clinical Trial Management

Kura Oncology

Boston, MA, United States
Base: $228,000 - $252,000 py; bonus/equity: annual...
On-site
Leading large phase 3 clinical trials
Clinical trial budget management
Gcp and ich guidelines knowledge
Kura Oncology is committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines

Job Summary

  • Kura Oncology is committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines.
  • The Director will lead complex global clinical trials, manage clinical operations teams, and ensure compliance with regulatory standards while fostering a collaborative culture.
  • The compensation package includes a competitive base salary, bonus, equity, 401K with employer contributions, generous PTO, and various employee benefits.

Matching Summary

Kura Oncology is committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines.

Salary

Base: $228,000 - $252,000 per year; Bonus/Equity: Annual target bonus and generous stock options; Benefits: 401K, PTO, holidays, paid parental leave, and comprehensive benefits package

Skills & Requirements

Must-have

  • Leading large Phase 3 clinical trials
  • Clinical trial budget management
  • GCP and ICH guidelines knowledge
  • Managing CROs and external vendors
  • Cross-functional team collaboration
  • Clinical operations leadership

Nice-to-have

  • Analytical problem-solving skills
  • Adaptability to changing priorities
  • Strong communication skills
  • Experience with IND and NDA submissions
  • Experience setting up trials outside US and Europe
  • Proficiency with Microsoft Project
  • Fostering collaborative culture

Key Requirements

  • Bachelor’s degree in science or healthcare
  • 10+ years leading Phase 3 oncology/hematology trials
  • Experience managing contracts and clinical finance
  • Flexibility to travel domestically and internationally
  • In-depth knowledge of GCP and ICH guidelines
  • Experience with IND and NDA submissions

Work Rights

Not specified

Tailored Resume

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