At ICON, it's our people that set us apart.
Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity.
We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point.
In short, to be the partner of choice in drug development.
That's our vision.
We're driven by it.
And we need talented people who share it.
If you're as driven as we are, join us.
You will be working in a dynamic and supportive environment with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
As a Site Management Associate at ICON, you will be responsible for managing, implementing, and monitoring clinical studies, with support, in a team setting within a global organization.
Following an initial training period, you will begin working on large global projects within a variety of therapeutic areas.
The work of a Site Management Associate is varied and challenging whilst offering you the opportunity to use your language skills.
Your responsibilities will include:Identifying, training/initiating, and closing out study sitesConducting remote site monitoring visits and/or targeted on-site visits as neededTraining Site Staff on essential processes and systemsCollection and management of essential documentsManaging study sites and the required protocols, amendments, and/or deviations, assuring that data is reported accurately and timelines are maintainedServing as the primary point of contact for Investigator site staffPerforming study trackingYou will be working within a project and team-based environment with both internal and external stakeholders.
Given the client-focused and fast-paced nature of the Site Management Associate position, we are looking for proactive individuals who have a keen eye for detail.
What you need:Some experience working within a CRO, Pharmaceutical, or hospital/healthcare environment would be preferred but is not essentialStrong verbal and written communication skills are required, and fluency in Spanish and English and at least one additional European language such as German or Dutch is preferred but all languages can be consideredWe would also welcome some previous experience as a CRA or an In-house CRA.Benefits of Working in ICON:Our success depends on the quality of our people.
That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages, and to keep them competitive, we regularly benchmark them against our competitors.
Our annual bonuses reflect delivery of performance goals - both ours and yours.
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