We currently have an exciting new opportunity for an Associate Project Manager to join our growing team, sponsor dedicated.
The Associate Project Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management.
This is a permanent role with ICON on FSP and fully home-based. You must be located in the following countries to be consider: Bulgaria, Poland OR Spain.
Start date: June, July and August 1st 2025
You MUST come from a Clinical Research background
CRA backgrounds are not considered.
Job profiles that would be considered:
Are you ready to take your career to the next level as an Associate Project Manager with ICON? This is an amazing opportunity to join a vibrant and dedicated team in the BioPharmaceuticals Clinical Operations space. In this fully home-based role, you’ll be an integral part of the global study team, supporting the delivery of crucial clinical studies. If you’re in Bulgaria, Poland, or Spain, we want to hear from you! As an Associate Project Manager, your responsibilities will include preparing key study documents, maintaining smooth interactions with internal and external partners, and contributing to the planning of vital meetings. You’ll also ensure timely supply of Investigational products while effectively managing risks. Your expertise will help maintain high-quality standards in the Trial Master File and support budget management for our Global Study Directors. With at least three years of experience in the pharmaceutical industry or academic environment, coupled with your project management skills, you will thrive in this collaborative and fast-paced setting. If you're passionate about clinical research and looking to grow your career in a supportive environment, this role with ICON could be the perfect fit for you. Join us and help shape the future of clinical studies, where your efforts will help drive efficiency and excellence every step of the way!
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