Job Description
Clinical Research Study Coordinator
n
Brisbane's south-western corridor | Hybrid flexibility
n
Are you an experienced Study Coordinator ready to take genuine ownership of your clinical trials?
n
This is an opportunity 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.
n
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.
n
The role
n
Reporting directly to the Clinical Operations Lead, you will independently coordinate clinical trials from site activation through to close-out.
n
Your responsibilities will include:
n
n
Coordinating patient visits in accordance with study protocols
n
Identifying and phone-screening potential participants
n
Supporting the informed consent process
n
Performing phlebotomy, ECGs, vital signs and sample processing
n
Maintaining accurate source documentation and entering data into EDC systems
n
Managing sponsor portals, study documentation and patient status trackers
n
Coordinating investigational product and drug accountability
n
Responding to data queries and supporting monitoring visits
n
Identifying and documenting adverse events and serious adverse events
n
Communicating with sponsors, CROs, investigators and study participants
n
Keeping multiple studies, deadlines and competing priorities on track
n
n




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

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