Clinical Trial Manager
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development
As a Clinical Trial Manager at ICON (FSP), you will be embedded within a dedicated sponsor partnership, providing country-level operational leadership and oversight for clinical trials. You will be accountable for delivering assigned studies in line with sponsor procedures, ICON quality standards, ICH‑GCP, and applicable regulatory requirements.
This role represents ICON within the sponsor organisation and requires strong collaboration, consistency, and ownership to ensure successful trial delivery within a matrixed FSP environment.
What You Will Do
In this role, you will be responsible for the end‑to‑end operational delivery of clinical trials at country level, working closely with sponsor global and local teams.
Key responsibilities include:
- Provide country-level leadership for assigned clinical trials within an FSP model, delivering against sponsor timelines, quality, and operational commitments
- Act as the primary country operational interface between ICON and sponsor study teams, escalating risks and issues appropriately
- Plan, coordinate, and oversee site feasibility, selection, qualification, initiation, monitoring, co‑monitoring, and close‑out activities
- Ensure trial conduct complies with sponsor SOPs, ICON processes, ICH‑GCP, and local regulatory requirements
- Lead and support CRAs and study support staff assigned under the FSP model, promoting performance, consistency, and quality
- Proactively identify, assess, and manage country and site‑level risks, implementing mitigation and corrective actions in collaboration with sponsor stakeholders
- Review monitoring documentation, study metrics, and reports to ensure data quality, compliance, and inspection readiness
- Support recruitment delivery through collaboration with investigators, sites, and sponsor stakeholders
- Contribute to country-level planning, forecasting, and execution of timelines, resources, and operational deliverables
Required qualifications and experience:
- Bachelor’s degree in life sciences, or a related discipline
- Proven experience in clinical research, including senior CRA, lead CRA, or trial management responsibilities, preferably within an FSP or sponsor‑dedicated model
- At least 3–5 years of experience in project or clinical trial management, with experience in cardiovascular and respiratory therapeutic areas being desirable
- Strong working knowledge of ICH‑GCP, clinical trial regulations, and country‑specific requirements
- Demonstrated ability to manage multiple studies, stakeholders, and priorities within a matrixed operating environment
- Strong communication, organisational, and risk‑management skills
- Willingness to travel nationally and internationally in line with study requirements
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:
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize 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.
Visit our careers site to read more about the benefits ICON offers.
At 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, color, 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 or submit a request here.
Interested 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.
Are you a current ICON Employee? Please click here to apply
