Executive Director, Asset Development Team Leader

539

Base: $310,900.00 - $489,400.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
5 years industry drug development experience
5 years clinical experience required
Phase 3 or registrational study design
The Executive Director of the Asset Development Team at 539 is responsible for leading the strategy and execution of drug development activities for oncology products, ensuring alignment across scientific, commercial, and manufacturing sectors. The ideal candidate will have significant experience in drug development and clinical trial management, particularly in oncology, with a strong focus on strategic leadership and regulatory interactions

Job Summary

  • The Executive Director is responsible for the strategy, oversight, and delivery of end-to-end activities involving new or marketed drug(s) for oncology indications.
  • Candidates must have designed, executed, and reported out phase 3 or registrational studies with supported submission activities for labels.
  • The role offers a comprehensive benefits package including medical, dental, vision, retirement benefits, and an annual bonus eligibility.

Matching Summary

Match Score: 85

The Executive Director of the Asset Development Team at 539 is responsible for leading the strategy and execution of drug development activities for oncology products, ensuring alignment across scientific, commercial, and manufacturing sectors. The ideal candidate will have significant experience in drug development and clinical trial management, particularly in oncology, with a strong focus on strategic leadership and regulatory interactions.

Salary

Base: $310,900.00 - $489,400.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • 5 years industry drug development experience
  • 5 years clinical experience required
  • Phase 3 or registrational study design
  • Regulatory agency interaction expertise
  • Matrix structure navigation skills

Nice-to-have

  • Dose justification experience
  • BLA/sBLA global submission knowledge
  • Diagnostic use understanding
  • External KOL management
  • Multiple therapy modalities experience

Key Requirements

  • M.D. or MD/PhD degree
  • Board certified or eligible in oncology disciplines
  • Minimum 5 years industry experience in relevant therapeutic area
  • Minimum 5 years clinical experience
  • Experience leading submissions for labels and post-approval launch readiness

Work Rights

Not specified

Tailored Resume

Cover Letter