Director, Gco Program Lead (gcpl)

BeOne Medicines

Remote
$171,900.00 - $231,900.00 annually; annual bonus p...
Remote
Global program management skills
Therapeutic area expertise
Clinical operational planning
BeOne Medicines is seeking a Director, GCO Program Lead (GCPL) for a remote position, focusing on strategic operational planning and clinical performance in cancer research. The ideal candidate should possess extensive experience in clinical trials, strong leadership skills, and a collaborative spirit, aligned with the company's mission to fight cancer

Job Summary

  • The GCO Program Lead is accountable for the strategic operational planning and clinical operational performance of designated programs and acts as a point of escalation for issue resolution.
  • This role involves leading gCSMs, providing mentorship, and partnering with other R&D representatives to drive disease/asset strategy and ensure execution excellence.
  • Responsibilities include strategic leadership, program management, budget forecasting, oversight of study execution, and fostering a global mindset across Clinical Operations.

Matching Summary

Match Score: 85

BeOne Medicines is seeking a Director, GCO Program Lead (GCPL) for a remote position, focusing on strategic operational planning and clinical performance in cancer research. The ideal candidate should possess extensive experience in clinical trials, strong leadership skills, and a collaborative spirit, aligned with the company's mission to fight cancer.

Salary

$171,900.00 - $231,900.00 annually; Annual bonus plan; Comprehensive benefits package

Skills & Requirements

Must-have

  • Global program management skills
  • Therapeutic Area expertise
  • Clinical operational planning
  • Clinical operational performance
  • Global team leadership
  • ICH/GCP Guidelines knowledge

Nice-to-have

  • Scientific and business professionals
  • Highly motivated, collaborative
  • Passionate interest in fighting cancer
  • Borderless leadership
  • Talent development
  • Process improvement initiatives

Key Requirements

  • 10+ years experience in clinical trial industry
  • Bachelor or higher degree in scientific or healthcare discipline
  • Project management experience across entire lifecycle of multi-region/country clinical trials
  • Experience in people management and program management preferred

Work Rights

Not specified

Tailored Resume

Cover Letter