PM
- LocationAustralia, Sydney
- Work typeRemote
- EmploymentFull-time
- Posted14 November 2026
- SourceICON's careers page (Workday)
Last checked11 min ago: still listed on ICON's careers page. First seen 11 min ago.
Moves fastWhen ICON takes a role down early, it is usually about 8 days after posting. Apply soon.
At a glance
- Skills and toolsGoogle Cloud
Read from the ad by RoleFinder, with rules and an AI reading; the description is the source.
About the role
Clinical Trial Manager, Sydney At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.
What You Will Do:
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
- Develop and maintain integrated study plans, timelines and operational controls.
- Coordinate cross functional study activities and dependencies.
- Monitor quality, risks, issues and milestones and drive corrective action.
- Oversee vendors, sites or functional contributors within assigned scope.
- Maintain clear sponsor, client and stakeholder reporting.
Required qualifications and experience
- Relevant life sciences, healthcare or clinical research qualification, or equivalent relevant clinical trial experience.
- Experience coordinating or managing clinical studies across multiple functions, sites or vendors.
- Working knowledge of ICH Good Clinical Practice (GCP) and clinical trial lifecycle activities.
- Experience using clinical trial management, reporting or study planning systems.
- Experience developing and maintaining integrated study plans, timelines and operational controls.
- Experience coordinating cross functional study activities and dependencies.
- Experience monitoring quality, risks, issues and milestones and driving corrective action.
Preferred qualifications and experience
- Prior monitoring experience.
- Experience leading global or multiregional studies.
- Formal project management training or certification.
- Therapeutic area expertise relevant to assigned studies.
Working conditions
- Willingness to travel as required (approximately 25%).
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- 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
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
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 .
Are you a current ICON Employee? Please click here to apply
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