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 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.

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
- Strong 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 0410 942 *** or

n

***email_hidden***

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