Live opening · Posted 7 hours ago

Project Associate

ICON plc · US, Blue Bell (ICON)
Workday
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At a glance

The key details from the original listing.

Posted 7 hours ago
CompanyICON plc
LocationUS, Blue Bell (ICON)
SourceWorkday
ListedPosted 7 hours ago

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About the role

Description supplied by the original job listing.

Clinical Trial Associate
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 Project Associate at ICON, you will provide key administrative support in clinical operations and project management, ensuring projects align with contract and client expectations.
What You Will Do:
Your role will involve delivering executive support and administration work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
Organizing project team and client meetings, including scheduling, preparing meeting materials, binders, agendas, and minutes.
Managing study information and supplies, generating and maintaining essential documents like organizational charts, team calendars, newsletters, and project-specific information.
Overseeing internal and client project reporting, ensuring accuracy in reports for project status and financial tracking, along with system updates and queries.
Supporting the project manager with financial tasks, including managing the purchase order process and processing study invoices and Investigator payments.
Preparing and maintaining study files, ensuring compliance with filing/naming guidelines in the electronic trial master file, and tracking document status.
Your Profile:
You will bring relevant executive support and administration experience, along with the following qualifications and skills.
Required qualifications and experience:
Bachelor's degree or international equivalent in business, finance, health sciences, or related field, preferred.
Experience in a CRO, pharmaceutical company, or in clinical research is an advantage.
Proficiency in computerized information systems and standard application software, including MS Office.
Strong skills in MS Word, PowerPoint, Excel, and Outlook, with experience in maintaining Excel trackers and building PowerPoint slides.
Experience in taking meeting minutes and facilitating and scheduling MS TEAMS meetings is preferred.
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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