Clinical Research Coordinator

GenesisCare

St Leonards

5 days ago

St Leonards

5 days ago

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Clinical Research Coordinator

GenesisCare seeks a Clinical Research Coordinator for a 14-month maternity leave contract at their St Leonards site in Australia. The role involves coordinating clinical trials in oncology, ensuring compliance with GCP and regulatory standards, and collaborating with investigators and stakeholders.

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On-site

Full-time

Entry Level

Good Clinical Practice (GCP)

Clinical Trial Regulations

Salary

Not specified

Work Location

St Leonards, New South Wales, Australia, AU

Work Model

On-site

Experience Required

2 years

Employment Type

Full-time

Experience Level

Not Applicable

Contract Length

14 months

Core Qualifications

Technical (Must-have)

Good Clinical Practice (GCP)clinical trial regulations

Soft Skills

organisationattention to detailcommunicationinitiativeflexibilityteamwork

Tools (Must-have)

MS Officeclinical trial software

Key Responsibilities

•Coordinate and deliver clinical research activities in accordance with study protocols, GCP guidelines, and regulatory requirements
•Work closely with Principal and Co-Investigators to support day-to-day management of clinical trials
•Support study start-up, participant recruitment, study visits, monitoring, and close-out activities
•Maintain accurate study documentation, regulatory files, and timely data entry
•Perform protocol-specific study visits and clinical tasks (vitals, ECGs, venepuncture, sample processing)
•Act as key point of contact for study participants, sponsors, and internal stakeholders
•Liaise with hospital departments, third-party providers, and sponsor representatives
•Prepare for, host, and respond to monitoring and site visits
•Complete mandatory and trial-specific training, contribute to quality, safety, and compliance activities

Clinical Research Coordinatoroncologyclinical trialsGCPSt LeonardsAustraliafull-timecontractmaternity leave cover

Key Responsibilities

•Coordinate and deliver clinical research activities in accordance with study protocols, GCP guidelines, and regulatory requirements

•Work closely with Principal and Co-Investigators to support day-to-day management of clinical trials

•Support study start-up, participant recruitment, study visits, monitoring, and close-out activities

•Maintain accurate study documentation, regulatory files, and timely data entry

•Perform protocol-specific study visits and clinical tasks (vitals, ECGs, venepuncture, sample processing)

•Act as key point of contact for study participants, sponsors, and internal stakeholders

•Liaise with hospital departments, third-party providers, and sponsor representatives

•Prepare for, host, and respond to monitoring and site visits

•Complete mandatory and trial-specific training, contribute to quality, safety, and compliance activities