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Project Associate

  1. Multiple US Locations
JR114014
  1. ICON Full Service & Corporate Support
  2. Project/ Program Management

About the role

This vacancy has now expired. Please click here to view live vacancies.

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.


With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.


Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The Role

We are seeking a Project Associate to join our team within the Biotech, Government, and Public Health division at ICON. In this role, you'll provide key administrative support in clinical operations and project management, ensuring projects align with contract and client expectations. You'll also be instrumental in designing and analyzing clinical trials and interpreting medical data, contributing significantly to innovative healthcare advancements.

What you will be doing:

  • 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:

  • Bachelor’s degree or international equivalent in business, finance, health sciences, or related field, preferred.
  • 1-2 Year of Adminstrative Experience Required
  • Adminstrative 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.

If you're a detail-oriented and driven individual thriving in fast-paced environments, this opportunity is for you. Known for surpassing deadlines and constantly seeking improvement, you're ready to expand your skills in the CRO industry. We offer a role that combines professional growth with a balanced work-life approach, in a team as passionate as you are. If this speaks to your career aspirations, we invite you to apply today!

Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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 through the form below.

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