Clinical Research Coordinator

GenesisCare

Murdoch

1 week ago

Murdoch

1 week ago

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Clinical Research Coordinator

GenesisCare seeks a Clinical Research Coordinator for a 12-month full-time opportunity at Fiona Stanley Hospital in Murdoch, Western Australia. The role involves coordinating clinical trials, working with investigators and multidisciplinary teams to deliver high-quality research. Requires at least two years of nursing, research, or scientific experience and a relevant undergraduate degree.

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On-site

Full-time

Mid Level

Good Clinical Practice (GCP)

Clinical Trial Regulations

Salary

Not specified

Work Location

Murdoch, Western Australia, Australia, AU

Work Model

On-site

Experience Required

2 years

Employment Type

Full-time

Experience Level

at least two years’ experience in nursing, research, or a scientific setting

Contract Length

12 months

Core Qualifications

Technical (Must-have)

Good Clinical Practice (GCP)clinical trial regulationsvenepuncturesample processingECGs

Soft Skills

communicationteamworkorganizational skillsattention to detailinitiativeflexibilityrelationship buildingtime management

Tools (Must-have)

MS Officeclinical trial software

Key Responsibilities

•Coordinate and deliver clinical research activities in line with study protocols, Good Clinical Practice (GCP) guidelines, and all regulatory requirements
•Partner closely with Principal and Co-Investigators to manage day-to-day trial activities
•Support efficient study start-up, participant recruitment, study visits, monitoring, and close-out activities
•Maintain accurate and complete study documentation, regulatory files, and data entry within required timelines
•Conduct protocol-specific study visits and clinical tasks (e.g. vitals, ECGs, venepuncture, sample processing) as deemed competent
•Act as a key point of contact for study participants, sponsors, and internal stakeholders
•Liaise with hospital departments, third-party providers, and sponsor representatives to ensure smooth trial delivery
•Prepare for and host monitoring and site visits, addressing queries in a timely manner
•Complete mandatory and trial-specific training and contribute to quality, safety, and compliance activities

Clinical ResearchClinical TrialsHealthcareResearch CoordinatorGCPFiona Stanley HospitalFull-timeContractOn-siteAustralia

Key Responsibilities

•Coordinate and deliver clinical research activities in line with study protocols, Good Clinical Practice (GCP) guidelines, and all regulatory requirements

•Partner closely with Principal and Co-Investigators to manage day-to-day trial activities

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

•Maintain accurate and complete study documentation, regulatory files, and data entry within required timelines

•Conduct protocol-specific study visits and clinical tasks (e.g. vitals, ECGs, venepuncture, sample processing) as deemed competent

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

•Liaise with hospital departments, third-party providers, and sponsor representatives to ensure smooth trial delivery

•Prepare for and host monitoring and site visits, addressing queries in a timely manner

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