Clinical Trial Coordinator, Office-based in Sydney

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Clinical Study Coordinator at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include

- Collaborating with cross-functional teams to develop and implement clinical trial protocols.
- Coordinating and overseeing the execution of clinical studies,



ensuring adherence to protocols and regulatory requirements.
- Managing study timelines, budgets, and resources effectively.
- Facilitating communication between investigative sites, sponsors, and internal teams.
- Ensuring data accuracy and completeness through regular monitoring and quality control activities.

Your Profile: You will bring relevant clinical research experience, along with the following qualifications and skills.

Required qualifications and experience

- Bachelor's degree in a relevant scientific discipline.
- Proven experience as a Clinical Study Coordinator or in a similar role.
- Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Solid organizational and multitasking skills.
- Excellent communication and interpersonal abilities.

📌 Clinical Trial Coordinator (Australia)
🏢 Nextrials
📍 Australia