Monitor progress of clinical studies at investigative sites
Ensure studies are conducted, recorded, and reported per protocol and ICH-GCP
Coordinate study setup and monitoring activities (investigators, submissions, visits)
Travel to sites for monitoring visits; up to 50–60% travel
Work in a smaller CRO with direct line management and impact
Voice heard and influence decisions in a collaborative environment

🎯 Requirements

Life science degree or equivalent experience
1+ year as a CRA in CRO or pharma/biotech
Experience managing oncology studies
Availability for domestic travel up to 50–60% (intl travel may occur)
English fluency and local language proficiency where based
Excellent communication and organizational skills; team player

Apply on employer's website

This employer gathers applications via their own applicant tracking system.

You will be redirected to an external application form.

Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Healthcare Jobs. Just set your preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.

Activate JobCopilot