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CRA (Oncology experience required)

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About the role

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Clinical Research Associate
 
This is an opportunity to work for ICON’s Clinical Research division as a CRA within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. 
 
Overview of the Role
 
Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.  You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. 
Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.  
Depending on your level of experience, you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects. 
 
Role Requirements  
 
Previos Vaccines & Oncology experience are required for this role.
 
With a University degree in medicine, science, or equivalent; you will have previous monitoring experience in medium sized studies, including study start-up and close-out (for all roles above Entry Level).  You should also have knowledge of ICG GCP guidelines and the expertise to review and evaluate medical data.  
 
Fluent in English, as well as the local language.
 
You must be available to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving licence. 
 
The last day for applications will be on the 3rd November 2014.
 
*LI-PG1
 
 
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