Director, Clinical Study Management (contract)

Eikon Therapeutics

Millbrae, CA, USA
On-site
Clinical trial regulations and gcp
Oncology clinical development experience
Oversight of clinical vendors
Manage all aspects of clinical operations study management for assigned Eikon clinical programs, ensuring exquisite inhouse execution of all interventional clinical trials and oversight of requisite clinical vendors

Job Summary

  • Manage all aspects of clinical operations study management for assigned Eikon clinical programs, ensuring exquisite inhouse execution of all interventional clinical trials and oversight of requisite clinical vendors.
  • Support the systematic pursuit of optimal performance, efficiency, and quality across all aspects of clinical study management via a focus on operational excellence, adhering to GCP and relevant policies.
  • This role requires a minimum of 3 days a week of onsite presence in either Jersey City, New Jersey or Millbrae, California offices.

Matching Summary

Manage all aspects of clinical operations study management for assigned Eikon clinical programs, ensuring exquisite inhouse execution of all interventional clinical trials and oversight of requisite clinical vendors.

Skills & Requirements

Must-have

  • Clinical trial regulations and GCP
  • Oncology clinical development experience
  • Oversight of clinical vendors
  • Inspection ready studies
  • Matrix organization collaboration

Nice-to-have

  • Agile of mind
  • Systematic and collaborative leader
  • Passion for operational excellence
  • Advancing patient care

Key Requirements

  • 12+ years with Bachelor's or 10+ years with Master's
  • Significant international oncology clinical studies experience
  • Proven track record with global regulatory submissions
  • Significant management experience in clinical trials
  • Complete understanding of ICH GCP

Work Rights

Not specified

Tailored Resume

Cover Letter