Clinical Program Manager, Oncology

Eikon Therapeutics

Millbrae, CA, USA
On-site
Plan and oversee clinical trials
Cross-functional team collaboration
Ich-gcp and regulatory compliance
Plan and oversee the execution of clinical trials in oncology and other therapeutic areas, ensuring studies are delivered on time and within budget with a strong focus on quality and operational excellence

Job Summary

  • Plan and oversee the execution of clinical trials in oncology and other therapeutic areas, ensuring studies are delivered on time and within budget with a strong focus on quality and operational excellence.
  • Lead proactive risk identification, assessment, and management, driving alignment on mitigation strategies and serving as a central point of contact for cross-functional team effectiveness.
  • Lead, manage, hire, develop, and mentor global and regional Clinical Study Management personnel, contributing to improvement initiatives and operational excellence.

Matching Summary

Plan and oversee the execution of clinical trials in oncology and other therapeutic areas, ensuring studies are delivered on time and within budget with a strong focus on quality and operational excellence.

Skills & Requirements

Must-have

  • Plan and oversee clinical trials
  • Cross-functional team collaboration
  • ICH-GCP and regulatory compliance
  • Vendor relationship management
  • Study budget and timeline management
  • Risk identification and mitigation

Nice-to-have

  • Passion for advancing patient care
  • Solutions oriented and flexible
  • Growth mindset and independent work

Key Requirements

  • Bachelor's degree with 8 years of experience
  • Master's degree with 6 years of experience
  • PhD with 3 years of experience
  • Fluency in English
  • In-depth knowledge of ICH-GCP
  • Proficiency in clinical trial management systems
  • PMP certification preferred

Work Rights

Not specified

Tailored Resume

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