Clinical Trial Management Associate, Oncology (emea/latam)

Eikon Therapeutics

Millbrae, CA, USA
On-site
Clinical trial execution and oversight
Site start-up coordination
Trial master file (tmf) management
Serve as a critical inhouse clinical operations partner in the execution, and oversight of Phase I–III global oncology clinical trials

Job Summary

  • Serve as a critical inhouse clinical operations partner in the execution, and oversight of Phase I–III global oncology clinical trials.
  • Independently manage assigned study responsibilities and help ensure the delivery of high-quality, compliant, and timely trial data.
  • This role requires fluency in one of the following languages: Portuguese, German, Italian, French, Polish.

Matching Summary

Serve as a critical inhouse clinical operations partner in the execution, and oversight of Phase I–III global oncology clinical trials.

Skills & Requirements

Must-have

  • Clinical trial execution and oversight
  • Site start-up coordination
  • Trial Master File (TMF) management
  • Investigational product tracking
  • ICH-GCP and FDA compliance

Nice-to-have

  • Operational mindset
  • Flexible and collaborative spirit
  • Passion for drug development

Key Requirements

  • 3+ years of relevant clinical trial experience (Bachelor's)
  • 1-2 years of experience (Master's)
  • Fluency in Portuguese, German, Italian, French, or Polish
  • Minimum 3 days per week onsite

Work Rights

Not specified

Tailored Resume

Cover Letter