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Hybrid coordinator role running phase II and III oncology trials, open until filled.
$105,000 – $120,000 per year
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.
Prepare HREC submissions; coordinate site activation; maintain trial master files; liaise with sponsors.
Life-sciences degree; two or more years in clinical research; working knowledge of ICH-GCP.