Remote Senior Director: Oncology Clinical Programs

Menarini Group

New York (NY)

Remote

USD 220,000 - 270,000

Full time

14 days+

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Benefits offered by this job

Fidelity 401(k) with company match
Medical insurance (Anthem PPO/HDHP)
Life & AD&D insurance
Pre-tax FSA/HSA programs

Job summary

Menarini Stemline is seeking a Senior Director of Clinical Program Lead to oversee regional clinical operations across multiple studies in a US-remote setting. You will lead cross-functional teams, manage timelines, budgets, and CRO/vendor performance, and ensure adherence to GCP and FDA regulations.

The role reports to Global Clinical Operations and requires 15+ years in drug development with oncology experience, matrix leadership, and strategic program management across US and global programs.

Qualifications

  • BS/BA degree in a scientific or health-related discipline; advanced scientific or equivalent experience preferred.
  • Experience leading teams in APAC region is desirable.
  • 15+ years in drug development, clinical research and operational strategy, preferably in biotech/pharma.

Responsibilities

  • Leads multiple clinical studies in parallel via direct reports and/or vendors.
  • Manages study execution with/without a CRO, ensuring on-time enrollment and completion.
  • Supports cross-functional partnerships; directs core team and resolves issues.
  • Optimizes trial design and execution; reports study performance metrics regularly.
  • Oversees operational plans, budgets, and vendor relationships; ensures data integrity.

Skills

Team leadership
Budget management
Program management
Cross-functional collaboration
Regulatory knowledge
GCP/FDA knowledge
Communication skills
Risk management
Talent development
Multi-therapy experience

Education

BS/BA in science/health

Job description

Menarini Stemline is seeking a Senior Director of Clinical Program Lead to oversee regional clinical operations across multiple studies in a US-remote setting. You will lead cross-functional teams, manage timelines, budgets, and CRO/vendor performance, and ensure adherence to GCP and FDA regulations.

The role reports to Global Clinical Operations and requires 15+ years in drug development with oncology experience, matrix leadership, and strategic program management across US and global programs.

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