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About the role ICON and you Application Process Day in the life Who we are

Site Activation Coordinator

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About the role

This vacancy has now expired. Please click here to view live vacancies.
 
Site Activation Coordinator
 
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.
 
As a Site Activation Coordinator you will be assigned to one of ICONs Global Key Accounts.
 
Position Summary:
 
As a Site Activation Coordinator you will provide general and specialised functional, administrative, organisational, reporting and coordinating support during site activation activities through all phases of the clinical trial lifecycle and in a manner that ensures timeframes, targets and the quality of the deliverables are in line with internal and external customer expectations.
 
You will work as part of a close and successful team, working with Study Start-Up and Site Activation colleagues to ensure optimised site activation and maintenance.
 
Role Requirements  
  • To perform this job successfully an individual must be able to perform each essential duty satisfactorily.  The requirements listed below are representative of the knowledge, skill and/or ability required.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Excellent organisational skills with capacity for high level attention to detail, demonstrating the following key competencies:
    • Critical thinker and solution focused
    • Proactive & Delivery focused
    • Client focused
    • Excellent planning and organisational ability
    • Analytical and data focused
    • Team focused & collaborative
    • Excellent communication skills
  • Direct experience and organismal and or administrative function or clearly demonstrates capacity to reach a high standard.  Ideally with proven experience in the management of projects and/or staff in a global/multi-regional environment.
  • Ability to successfully manage, positively interact and liaise successfully with all levels of staff at ICON, vendors and clients.
What’s Next
 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to 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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Day in the life

Two medics at ICON clinical research clinic
The Strategic Role of Site Selection and Activation in Clinical Trials

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