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- Provide Support to various projects
- Maintain and Tracking clinical study documentation
- Coordinate study materials
- Collate relevant study information.
- Ability to work on study teams that are often virtual, multi-cultural, and multi-disciplinary
- Serve as the primary contact for sites and investigators participating in studies
- Act as a resource for internal study teams and other ICON departments
- Maintains, reviews, and ensures adequacy of information and data contained in site management reports, tracking systems (CTMS or others) and other site management documents
- Conduct and complete remote site management activities, with support as needed, according to applicable SOPs and the Site Management Plan
- 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
- Able to adapt to changes in deadlines, competing project demands and changes in the nature of assignments
- Ability to work independently with minimal direction ; successfully handles increasingly complex tasks/assignments PROBLEM SOLVING
- Demonstrate resourcefulness , makes appropriate use of available technology and tools in seeking and implementing solutions
- Work well with other individuals and departments to solve problems; anticipates problems and seeks solutions proactively WORK QUALITY
- Consistently produces high-quality work , with support
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Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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