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About the role

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Clinical Trial Assistant (CTA)
Location: Eastleigh
 
At ICON, it’s our people that set us apart.
As a global provider of drug development solutions, our work is serious business. But that doesn’t
mean you can’t have fun while you do it. With our vision to be the partner of choice in drug
development, we hire only the best and brightest in the industry.
 
Are you one of them?
As a Clinical Trial Assistant at ICON, you’ll work with a collaborative and successful team to support our Clinical Trial Management and Project Management teams with operational activities
. We pride ourselves on our amazing company culture, where we work as one team to achieve industry leading results.
 
The role
  • Provide Support to various projects
  • Maintain and Tracking clinical study documentation
  • Coordinate study materials
  • Collate relevant study information.
 
What you need
  • Strong Administrative skills·Organizational skills to support several team members.
  • Excellent written and verbal communication·
  • Working Knowledge of computer systems including
  • Microsoft Word, Excel, Outlook and PowerPoint
  • High school diploma or local equivalent
 
Why join us?
Ongoing development is vital to us, and as a CTA you will have the opportunity to progress your
career, with the potential to move into other related areas to enhance your skill set. Our benefits
package is competitive, our scope is international and we genuinely care about our people and their success.
 
ICON is an equal opportunity employer and committed to providing a workplace free of any
discrimination or harassment.
EOE race/color/religion/sex/sexual orientation/gender identity/disability/vet/national origin
 
 
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The Role of Data Management in Clinical Trials

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Introduction to Data Management in Clinical Trials In the field of clinical research, data management plays a crucial role in ensuring the success and accuracy of clinical trials. Clinical trials

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