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Job Description
- Req#: 118915
Lead global study teams with full ownership of study design, timelines, and budget
Oversee protocol development, execution, and reporting
Ensure data integrity, database closure, and compliance with regulatory standards
Collaborate with internal and external stakeholders, managing vendors and study sites
Support regulatory approvals and publication plans
Bachelor's in medical technology, chemistry, biology, or related field
Experience leading global clinical studies
Strong communication, leadership, and problem-solving skills
Proficient in Microsoft Office; statistical knowledge a plus
Deep understanding of GCP, ICH, and clinical lab standards
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
Overview
As a Study Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. We are looking for a Clinical Trial Manager who has managed IVD studies with Core LAB or Pathology experience!!
Responsibilities
What you will be doing:
Join our global team to lead and manage clinical studies that drive innovation in lab diagnostics. As a Clinical Study Manager, you'll be accountable for the planning, execution, and reporting of technical, clinical utility, and clinical performance studies—ensuring compliance, quality, and timelines.
Qualifications
You Are:
What ICON can offer you:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include:
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
About the company
We are a global healthcare intelligence partner with everything you need to take your assets from concept to compound to cure.