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Site Activation Coordinator

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About the role

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Study Activation Co-ordinator
 
This role can be based from any ICON office but we are also open to a homebased candidate within the EU region. 
 
This is an exciting entry level opportunity for a recent  Life Sciences graduate looking to develop a career within clinical trials.  You will work in a fast-paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.
 
Position Summary:
 
The Site Activation Coordinator will be assigned to one of ICONs Global Key Accounts. Supporting the Site Activation/Study Start Up team, in a time-critical manner to meet clinical trial objectives in adherence with ICON/client KPI’s and quality standards.
 
As a Site Activation Coordinator, you will provide administrative and coordinating support for site activation activities through all phases of the clinical trial lifecycle.  This role will have you working with many internal and external departments including our sponsors so you will be a great communicator with fluency in English both written and spoken.  You will undertake reporting activities so good level of excel will be essential as well as a general enthusiasm for learning and using new systems.  You will enjoy working with documentation and will maintain high levels of accuracy whilst delivering in a timely way to meet real deadlines.
 
If you feel you have an interest in developing a career in a clinical trial environment and have a degree in Life Sciences, we look forward to hearing from you.
 
What’s Next?
 
Following your application, your details will be reviewed by one of our dedicated recruiters.  If successful, we will contact you and 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.
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