Project Manager, Imaging
About the role
This vacancy has now expired. Please click here to view live vacancies.
As the Project Manager, in this position you will work with internal and external partners to bring structure while implementing complex, project-based systems with increased efficiency in the delivery of all projects and services and in turn, enhanced client satisfaction.
Overview of Role
- Manage delivery of project specifications, in accordance with the contract, timelines, and study budgets
- Act as the point of contact on the project for our clients, and coordinate partners on your project
- Prepare and oversee meeting agendas, minutes and producing project reports
- Author study documentation (Imaging Manuals, Staffing Plans, Communication Plans, Procedure Manuals, etc)
- Hold oversight of the development/ review/ maintenance of all trial documentation (Charter, eCRF, SRS, Reviewer Training Manuals)
- Proactively manage changes in project scope, identify potential crises and devise contingency plans
- Lead internal project teams, communicate with sites/ CRA's, and mentor junior Associate Project Managers
- Participate in Business Development opportunities including proposal/budget development, bid defense meetings, and capabilities presentations
- Travel (approximately 10%) domestic/or international travel
- Other duties as assigned
Role Requirements
- Have experience within Project Management, including experience with hands-on Imaging
- Bachelor's Degree in Science, or other relevant discipline and appropriate experience
- Effectively lead teams and inspire others to achieve goals through innovation, quality and excellence
- Encourage team interaction, boost employee motivation and appreciate team contribution
- Organizational skills
- Problem solving, analytical and communication abilities
Benefits of Working in ICON
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. 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 - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
Benefits of Working in ICON :
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. 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.
ICON is an equal opportunity employer - M/F/D/V 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
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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.
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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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