Job Description

Job Summary

Our European activities are growing rapidly, and we are currently seeking 1 full-time, office-based Clinical Trial Assistant to join our Regulatory Submissions Technical Advisors team in Stirling, Scotland, supporting clinical trial activities. This position will work as part of a team to accomplish tasks and projects that are instrumental to the company\xe2\x80\x99s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Track, process and organize clinical trial documents and communications;
• Conduct quality control reviews of documents and clinical trial submissions;
• Upload documents in the EMA\xe2\x80\x99s Clinical Trials Information System (CTIS) portal;
• Perform a variety of support tasks for the Label Development and Regulatory Intelligence teams;
• Maintain database/spreadsheets to facilitate tracking of department activities;
• Develop understanding and perform tasks in accordance with assigned SOPs and policies;
• Perform other duties depending on the departmental needs.

• Experience in a detailed administrative role preferred
• Minimum of a high school diploma;
• Work experience in a health science setting preferred;
• Excellent organizational and prioritization skills;
• Great attention to detail;
• Knowledge of Microsoft\xc2\xae Office;
• Excellent oral and written communication skills in English language.

Medpace