Clinical Research CoordinatorPenrith, NSW | Part-TimeBrand-New Research Site | Growing National Clinical Research Network
A Unique Opportunity
Ready to take the next step in your clinical research career?
This is an exciting opportunity to join a newly established clinical research site in Penrith, where you will play a key role in shaping site operations, enhancing participant experiences, and delivering high-quality clinical trials from the ground up.
Whether you are an experienced Clinical Research Coordinator or a healthcare professional looking to transition into research, this role offers the chance to work in a collaborative, fast-growing environment with strong opportunities for professional development and career progression.
Why This Role Stands Out
Join a brand-new site and contribute to building processes and culture from day oneFlexible full-time or part-time arrangement to support work-life balanceWork in a supportive and collaborative clinical research environmentOpportunity to expand your responsibilities as the site growsGain exposure across diverse clinical trials and cutting-edge research studiesIdeal for nurses or health professionals transitioning into clinical research
The Role
As a Clinical Research Coordinator, you will be responsible for ensuring the smooth and productive conduct of clinical trials while maintaining the highest standards of participant care, data quality, and regulatory compliance.
Your responsibilities will include:
Coordinating day-to-day clinical trial activities in accordance with study protocols, ICH-GCP guidelines, and regulatory requirementsManaging participant recruitment, screening, informed consent, scheduling, and follow-up visitsProviding participants with clear, timely,



and supportive communication throughout the study journeyPerforming clinical procedures within scope, including vital signs, ECGs, and sample collection where requiredMaintaining accurate source documentation, Investigator Site Files (ISF), study logs, and electronic recordsEntering and managing study data using EDC and IRT systemsLiaising with investigators, sponsors, CROs, and Clinical Research Associates (CRAs) to ensure seamless study deliveryResponding to study queries and monitoring actions within required timelinesSupporting study milestone tracking, risk management activities, and quality improvement initiativesAssisting with supervision and delegation of tasks to Clinical Trial Assistants (CTAs)Ensuring participant safety through timely AE/SAE reporting and protocol compliance
About You
We are looking for a motivated and organised individual with a passion for clinical research and patient care.
You will bring:
A science-related qualification, preferably within medicine, nursing, or health sciencesMinimum 2-3 years' experience in clinical research coordination or a strong interest in transitioning into researchExcellent organisational, communication, and interpersonal skillsStrong attention to detail and commitment to high-quality data standardsExperience using EDC and IRT systems (desirable)Ability to manage multiple priorities and work both independently and collaborativelyA patient-focused approach with a commitment to delivering an exceptional participant experience
On Offer
Opportunity to grow with an expanding clinical research networkSupportive leadership and ongoing professional developmentExposure to innovative and impactful clinical trialsStable working hours with improved work-life balanceCareer progression opportunities as the site expands
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📌 Clinical Research Coordinator (New South Wales)
🏢 Evolve Scientific
📍 New South Wales