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CRA II

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About the role

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ICON Clinical Research, Australia
Clinical Research Associate II
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. Working within a highly qualified team our Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV ensuring adherence to applicable regulations and principles of ICH-GCP.
 
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  
·      With a University degree in medicine, science, or equivalent; you will have at least 2 years of previous monitoring experience in medium sized studies, including SIV and close-out.  You should also have knowledge of ICG GCP guidelines and the expertise to review and evaluate medical data.   
·      Good command of English, as well as the local language, you will possess excellent written and verbal communication and interpersonal skills enabling you to deal with queries in a timely manner.  You should be able to produce accurate work to tight deadlines within a pressurised environment. 
·      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. 
·      You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.  
 

Benefits of Working in ICON

In comparison with our competitor’s and pharmaceutical companies, we provide more flexible and reasonable working platforms for coaching and educating new comer’s to be highly respected professionals in our industry. ICON also provides successful candidates with an excellent employment package and benefits adapted to the current job market.

 

We are more like an extended family with consideration of staff as individuals allowing a work-life balance.

 

 You would be joining us at the very right time – just when we won the Best Contract Research Organisation Award at the annual Scrip Awards 2017. 

If you would like more information please visit our company website: www.iconplc.com or careers.iconplc.com. Or feel free to email me directly: Jennifer.kim@iconplc.com  


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