Clinical Research Coordinator

An opportunity to join a boutique clinical organisation, who have had some healthy growth and are looking to ad an additional member to the team.

You will be working in a smaller team environment, joining a truly close-knit team. They push for a healthy work life and offer unique progression pathways across the business. Whether its across project management, clinical operations or having a niche SME specialism - and so presents a lot of opportunity for development in your career.

They are looking for a Clinical Research Coordinator to join on a permanent basis where you will be responsible for the full end-to-end management of multiple projects and so offers the chance to become a SME in a chosen therapeutic area. This is a patient focused role and will see you building strong relationships with both clinical patients and cross-functional research groups in the business.

This role would suit someone with a background in clinical research with strong experience across clinical trials.

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, ensuring 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, maintaining accurate and complete records.
• Liaise with study sponsors, principal investigators, and interdisciplinary teams to facilitate study implementation and resolve any issues that arise.
• 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 availability of necessary materials and equipment.
• Collaborate with study participants and provide education and support throughout the research process.

Qualifications:

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

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

Title: Senior Clinical Research Coordinator

Location: Melbourne (includes travel to Melbourne sites)

Salary: Circa $95,000 base plus superannuation (open to chat around salary uplifts, lets talk!)

Associated 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, Study coordination, Investigational drug/device, Study budgeting, Protocol amendments, Adverse event reporting, Data analysis, Good Clinical Practice (GCP), Study start-up, Site management