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About the Role
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.
Responsibilities
- 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.
Requirements
- Proven experience as a Clinical Study Coordinator or in a similar role.
- Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Strong organizational and multitasking skills.
- Excellent communication and interpersonal abilities.
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Location
- Sydney
Work Type
- Office-based
Education Level
- Bachelor's degree in a relevant scientific discipline.
Benefits
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
About the Company
- 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.
Equal Opportunity
- ICON is an equal opportunity employer.
- We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
- If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.