Clinical Study Coordinator ( Healthy Vounteers)

Join a state-of-the-art, well-equipped early-phase Clinical Trials Centre, dedicated to groundbreaking clinical research and improving patient outcomes.

Overview: We are seeking a motivated Clinical Study Coordinator to join this world-class clinical research centre with a state-of-the-art bedded facility to play a crucial role in managing clinical trial activities throughout the trial lifecycle, specifically early phase oncology clinical trial studies.

Key Responsibilities: As a Clinical Study Coordinator, you will coordinate and be involved in study-related meetings, including SIV and kick-off meetings, oversee and assist with the HREC submission process, and manage trial study expenses.

You have an opportunity to continuously develop personal skills and knowledge while contributing to the overall operational excellence including participating in site audits, managing responses to audit findings and Corrective and Preventative Actions (CAPA).

What we're looking for: Minimum 2-3 years experience as a Clinical Study Coordinator or Project management role. Patient-facing experience is essential.Early-phase Studies experience is preferred.Excellent planning, organizational, and time management skills.Adaptable and flexible to changing work environments and ability to maintain positive relationships with cross-functional stakeholders.Strong problem-handling skills and showcase proactiveness in managing complex issues. To be considered for this role you must be based in Sydney, Australia, and work on-site 5 days a week. This role offers a competitive salary package with salary sacrifice of up to $16k per year, meaning you can expense a portion of your salary on expenses to increase take-home pay.

We're always interested to hear from talented and engaging people like you. Get in touch and tell us about yourself.

#J-18808-Ljbffr