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About the Role

Oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Responsibilities

• Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
• Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Minimum 4-5 years of experience as a Clinical Research Associate.
• Strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously.
• Strong organizational and problem-solving skills.
• Proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills.
• Ability to influence and drive compliance within a complex environment.
• Willingness to travel as required (approximately 60%).
• Experience with healthy volunteers preferred.
• Must have the legal right to work in the country where the role is based.

Skills

• Clinical trial monitoring
• Quality and continuous improvement
• Site management
• Data integrity
• Stakeholder management

Location

• Melbourne, Australia

Work Type

• Full-time

Experience Level

• Senior
• Minimum 4-5 years

Education Level

• Bachelor's degree

Salary/Compensations

• Competitive base salary and performance related incentives

Benefits

• Health and wellbeing programmes
• 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

About the Company

• ICON is a global healthcare intelligence and clinical research organisation.
• Our mission is to bring new medicines and treatments to patients faster.
• We are a values-driven organisation where integrity, collaboration, agility, and inclusion are at the heart of how we work.

Equal Opportunity

• ICON is an equal opportunity employer.
• We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
• Reasonable accommodations are available during the recruitment process.