Clinical Trial Manager (Late Phase)
About the role
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At ICON, we are looking for specialist experience in Late Phase clinical studies to run Clinical Trial Management.
As a Clinical Trial Manager at ICON, lead clinical deliverables, oversee a global clinical team within Phase IIIb-IV projects. Act as the point of contact for the internal team and client, develop the clinical plan, implement protocol training requirements and maintain key clients relationships.
Your responsibilities will include:
- Lead the global team clinical team (including CRA's) on projects, providing the team with direction guidance
- Build in all necessary project training built in for assigned clinical staff and track relevant clinical project deliverables, use appropriate tracking and budgeting tools
- Update the sponsor clinical team with key aspects of the project actions and updates
What you need
- ICON is seeking experience in delivering late phase clinical studies as a CTM
- University/Bachelor's Degree in medicine, science or equivalent degree/experience
- Thorough understanding of ICH GCP and relevant regulations for the conduct of clinical trials
- Experience in Study Start Up preferred
- Due to the nature of this position, the employee will travel approx. 25%. Therefore, dependent on the employee's location, the employee may be required to possess a valid Driver's license
This position is open to be based in our ICON locations in Poland, Spain, Italy or UK, and includes flexibility to work full or part-time home based, depending on your proximity to an ICON office.
Benefits of Working in ICON
Other than working with a great team ambitious people, we also offer a very competitive salary and benefits package that includes an excellent pension scheme, private health care, life assurance and staff recognition schemes. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people, as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
What's Next?
Following your application, you will be contacted by one of our dedicated recruiters, and, if successful, we will be able to provide you with more details about this opportunity!
ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
Teaser label
IndustryContent type
BlogsPublish date
12/01/2025
Summary
How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
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BlogsPublish date
11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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