CRA I

Clinical Research Associate I

Sydney – Office based

Role Responsibility

Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies in phases II – III ensuring that applicable regulations and principles of ICG-GCP are adhered to

•   Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation

•   Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested

•   Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required

•   Managing sponsor generated queries efficiently and responsible for study cost effectiveness

•   Dependent on level of experience you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects 

Experience and Qualification 

•   1+ years of monitoring experience in phase I~III trials as a CRA

•   Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data

•   Fluent in English as well as the local language

•   Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner

•   Ability to produce accurate work to tight deadlines within a pressurized environment

•   Computer literate with Microsoft Office

•   Must be available to travel international and domestic at least 60% fly 

•   Must hold a bachelor’s degree in pharmacy, nursing, science, or equivalent

Benefits of Working in ICON

Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package.  This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.   

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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