Remote role with occasional travel to Brisbane, CA HQ.
Ensure compliance with ICH-GCP in site monitoring.
Perform on-site and remote monitoring per the Clinical Monitoring Plan.
Verify source documents and data integrity (SDV) as required.
Write and submit investigational site reports; update tracking systems; escalate issues as needed.

🎯 Requirements

Bachelor's degree in life sciences, RN, or equivalent.
3+ years in clinical trials; in vitro diagnostics experience.
Regulatory knowledge and GCP.
Multi-task, shift priorities, and solve problems.
Interpersonal, collaborative, and time management skills.
Excellent organizational skills; detail-oriented.
Veeva Vault/Medrio proficiency; strong comms; CRA cert or cancer detection exp preferred.

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