Clinical Trial Manager - Barwon Health

• Barwon Health + hybrid work arrangements
• 0.8 Part-time and 12 months fixed term
• HEW 8 $118,801 - $136,018 + 17% Superannuation

Why work with us?

At Deakin you will have access to benefits such as a variety of leave options including generous parental leave and the ability to purchase additional leave; flexible working arrangements to help manage your work-life balance; ongoing learning and development opportunities to grow your career; an inclusive and supportive culture and environment to work in, both online and on campus.

As a Clinical Trial Manager, you will:

• Lead end‑to‑end clinical trial governance, overseeing all regulatory, ethical, contractual and compliance requirements across a complex multi‑site trial.
• Drive strategic trial operations, including milestone planning, progress monitoring, recruitment oversight, safety and risk management, and GCP‑aligned implementation.
• Act as the central liaison for investigators, sponsors, clinicians and internal stakeholders, providing authoritative guidance and managing complex multi‑site communications.
• Build and lead a high‑performing multidisciplinary team while embedding strong quality assurance, audit readiness, continuous improvement and robust documentation systems.
• Foster inclusive, collaborative partnerships across the University and trial sites, using strong problem‑solving, change leadership and stakeholder engagement to deliver successful outcomes

To be successful, you’ll have:

• Postgraduate qualifications (or progress toward them) in a relevant health discipline, or extensive equivalent experience in clinical trials and research management.
• Proven experience coordinating multi‑site clinical trials, including recruitment, administration, data collection, safety monitoring and budget oversight.
• Strong understanding of clinical trial regulatory frameworks, ethics and governance processes, with the ability to design and implement risk‑assessment frameworks aligned with GCP.
• Excellent communication, organisational and analytical skills, with the ability to lead staff, manage timelines, resolve protocol deviations and respond to emerging trial issues.
• High digital literacy and data management capability, with strong time‑management skills and the ability to juggle multiple competing priorities effectively.

To apply click HERE