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Clinical Trials Coordinator

Hybrid coordinator role running phase II and III oncology trials, open until filled.

$105,000 – $120,000 / year

HybridFull timeNo clearanceHealthcare

About the role

Coordinate phase II and III oncology trials end to end — ethics submissions, site activation, participant scheduling, and data quality. Hybrid working with three days on site at the research campus.

Responsibilities

Prepare HREC submissions; coordinate site activation; maintain trial master files; liaise with sponsors.

Requirements

Life-sciences degree; two or more years in clinical research; working knowledge of ICH-GCP.