CTA

Clinical Trial Assistant

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. Our Clinical Trial Assistants (CTA's) play a key role within ICON.  Working closely with CRAs

Overview of the role

• You will need to ensure high levels of accuracy when completing tasks, you will set up, manage and maintain clinical study documentation.
• You will arrange and attend internal and external meetings, helping to produce presentation materials and generate meeting minutes. You will also assist in the tracking and distribution of safety reports and coordinate document translations if required.   
• Contacting external and internal individuals; you will collate relevant study information and assist with study payments.  You should be prepared to take on any additional tasks assigned as and when required. 

Role Requirements  

• You will possess sufficient administrative experience 
• You must possess previous working knowledge of Word, Excel, Outlook and PowerPoint. 
• You will be fluent in English and the local language for the country you are applying. You will have excellent communication skills, both written and verbal, enabling you to deal with queries in a timely manner.  A confident team player, your interpersonal experience will be the key to developing and maintaining relationships both internally and externally.  

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.  

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.