About the opportunity

The Clinical Trial Assistant will assist in the coordination of the interventional study activities and within the Study teams to ensure quality and consistency of the study deliverable to time, cost, and quality objectives.

Responsibilities

• Assist in coordination of clinical studies from the start-up to execution and close-out.
• Interface with Investigators, external service provider and CRAs during the collection process to support effective delivery of a study and its documents.
• Contribute to electronic applications/submissions by handling clinical-regulatory documents according to the requested technical standards
• Set-up, populate and accurately maintain information in tracking and communication tools

Skills & Experience

• Working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH/GCP guidelines
• Computer proficiency
• Minimum 2 years' experience as a CTA
• Very good knowledge of spoken and written English
• Good interpersonal skills and ability to work in a team environment
• Display excellent organisation and time management skills, excellent attention to detail, and ability to multi-task in a high-volume environment with shifting priorities

How to Apply

Click apply or contact Jill Manson, Recruitment Consultant at jmanson@hpgconnect.com for a confidential discussion.