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Study Start Up Associate

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About the role

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"At ICON, it's our People that set us Apart"
 
 
Do you have experience in a clinical research role and are now looking to develop your knowledge and career, focusing on study start up activities?
 
If so, working in this role may be the perfect move for you.  Serving as a primary contact for investigators and research coordinators, you will perform feasibility, site identification, site contract negotiation and other assigned study start up activities.  This will include the preparation, review and approval of country related ethics/regulatory submission packages and site level critical documents for Investigational Product (IP) release.  Some travel is anticipated, to attend Kick-Off, Investigator and/or study team meetings.
 
If you can demonstrate the ability to manage multiple tasks in a dynamic environment, with excellent organizational skills and attention to detail, ensuring the highest levels of customer satisfaction, please apply now.  
 
Benefits of working at ICON:
 
We provide our Study Start Up Associates with the resources to be successful and visible by enabling them to provide direct input/recommendations to senior management on the submission process and how it can be improved.
 
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.
 
Closing Date for Applications: Wednesday 10th September 2014
 
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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