Senior CTA
About the role
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- Independent, proactive, well organized and ready with the setting up of investigator site files for the site initiation visits
- Can think ahead and be ready
- Prepared and always up to date maintaining the study status progress and study CTMS systems
- Review and QC of study documents and ensure that the paper or electronic TMF is always audit ready
- Review study plans and manuals and support the project managers when required
- Taking meeting minutes
- Arrange translations and liaise other third party
- Organising printing of study documents and materials and any other visual aids used by the sites/patients
- Potential to assist in training and mentoring fellow CTAs and support the CTA supervisor
- High-school or A level Equivalent is mandatory,
- Previous high skill administration experience
- Worked at other CRO or Bio pharmaceutical is preference
- Intermediate working knowledge with Excel and Word
- Knowledge of ICH-GCP guidelines and ability to check quality of documents and pay attention to details
- Excellent written and verbal communication
- Ability to work to tight deadlines
- Ability to work with Remote team and follow written instructions
- Availability to travel up to 10% of the time
A better career. A better world. A better you.
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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