Clinical Research Coordinator

Join a thriving boutique clinical organisation that has experienced healthy growth and is looking to expand its team. This is a fantastic opportunity to work in a close-knit environment where collaboration and a healthy work-life balance are prioritised.

As a Senior Clinical Research Coordinator, you will be responsible for the full end-to-end management of multiple projects. You will have access to a range of trials and so will have a good variety of work.

This role will be an initial 12-month contract, looking to transfer to a permanent position at the end of the tenure.

Key Responsibilities:

• Coordinate and oversee all aspects of clinical research studies, ensuring compliance with protocols, regulations, and ethical guidelines.
• Recruit, screen, and enrol eligible study participants while maintaining accurate documentation and informed consent.
• Schedule and conduct study visits, procedures, and follow-up assessments according to study protocols.
• Collect, manage, and analyse research data, ensuring accurate and complete records.
• Liaise with study sponsors, principal investigators, and interdisciplinary teams to facilitate study implementation and resolve any issues.
• Assist in the preparation and submission of regulatory documents, including Institutional Review Board (IRB) applications and study amendments.
• Monitor and maintain study supply inventory, ensuring the availability of necessary materials and equipment.
• Collaborate with study participants, providing education and support throughout the research process.

Qualifications:

• Bachelor's degree in a health-related field, such as biology, nursing, or life sciences.
• A minimum of 2 years of experience as a Clinical Research Coordinator or in a similar research role is preferred.
• Strong understanding of clinical research processes, regulations, and ethical guidelines (e.g., ICH-GCP).
• Excellent organisational skills with the ability to multitask and prioritise effectively.
• Proficiency in data collection, management, and analysis.

If you are interested in this opportunity, please apply directly or contact Keeley Munday at 0283105854 or kmunday@i-pharmconsulting.com for more information.

Location: Melbourne (includes travel to Melbourne sites)
Salary: $75,000 - $100,000 base plus superannuation

Keywords: Clinical trials, Research protocols, Study coordination, Participant recruitment, Informed consent, Data collection, Study monitoring, Regulatory compliance, Ethical guidelines, Institutional Review Board (IRB), Research documentation, Investigational drug/device, Study budgeting, Protocol amendments, Adverse event reporting, Data analysis, Good Clinical Practice (GCP), Study start-up, Site management.