Cta2 (Luton) - Reading, United Kingdom - IQVIA
Description
Job Overview
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
Functions
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- Accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
- Collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports
Qualifications
- Third level degree
- 34 years administrative support experience.
- Minimum one year clinical research experience strongly preferred.
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
- Written and verbal communication skills including good command of English language.
- Basic knowledge of applicable clinical research regulatory requirement (GCP)
- Knowledge of applicable protocol requirements as provided in company training.
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