Clinical Research Study Coordinator
Brisbane's south-western corridor | Hybrid flexibility
Are you an experienced Study Coordinator ready to take genuine ownership of your clinical trials?
This is an prospect to join a close-knit clinical research team where the doctors are highly invested in research and the Study Coordinator plays a central role in delivering successful studies and creating an excellent patient experience.
Based in Brisbane's south-western corridor, the role offers flexibility to work remotely on non-clinic days. Onsite attendance is required for patient visits and home based work is coordinated around clinic requirements.
The role
Reporting directly to the Clinical Operations Lead, you will independently coordinate clinical trials from site activation through to close-out.
Your responsibilities will include:
Coordinating patient visits in accordance with study protocols
Identifying and phone-screening potential participants
Supporting the informed consent process
Performing phlebotomy, ECGs, vital signs and sample processing
Maintaining accurate source documentation and entering data into EDC systems
Managing sponsor portals, study documentation and patient status trackers
Coordinating investigational product and drug accountability
Responding to data queries and supporting monitoring visits
Identifying and documenting adverse events and serious adverse events
Communicating with sponsors, CROs, investigators and study participants
Keeping multiple studies, deadlines and competing priorities on track
Ethics and governance submissions are managed internally,



allowing you to focus on study delivery, patient care and trial coordination.
About you
You will ideally bring:
Previous experience coordinating clinical trials at site level
Current phlebotomy experience is essential
Confidence working independently and taking ownership of studies
Strong organisation and attention to detail
Experience managing sponsor systems, patient records and study documentation
Confidence conducting patient phone screens and supporting recruitment
The ability to build rapport with patients
Experience across cardiometabolic studies or a similar therapeutic area would be advantageous
Nursing qualifications or a strong clinical background would be highly regarded
Above all, you will be someone who sees clinical research coordination as a long-term career and enjoys being accountable for the successful delivery of your studies.
Why join?
Take genuine ownership of your clinical trials
Work closely with doctors who are actively engaged in research
Join an empowering environment where initiative is encouraged
Benefit from hybrid flexibility around clinic requirements
Make a visible contribution within a growing research operation
The successful candidate will ideally live in Brisbane's south-west, the western suburbs or within a manageable commute of the clinic.
The team is ready to move quickly and can accommodate an immediate start or notice period for the right person.
For more information reach out to Dana Sarkissian on ******** *** or
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#J-*****-Ljbffr

📌 Study Coordinator (Queensland)
🏢 i-Pharm Consulting
📍 Queensland