Provide study level administrative support to the clinical study management team, including running system reports and preparing status reports
Job Summary
Provide study level administrative support to the clinical study management team, including running system reports and preparing status reports.
Perform centralized monitoring activities on assigned sites to evaluate quality and integrity, and manage operational insights of assigned sites/studies.
Facilitate early identification of site-level risks and monitor site performance, making recommendations for timely corrective actions.
Matching Summary
Provide study level administrative support to the clinical study management team, including running system reports and preparing status reports.
Skills & Requirements
Must-have
Centralized monitoring activities
Subject Level Data Review
Clinical trial systems knowledge
Czech and Slovak language proficiency
Good Clinical Practice knowledge
Nice-to-have
Results and detail-oriented approach
Problem-solving skills
Effective working relationships
Strong telecommunication skills
Key Requirements
2 to 5 years of work experience
1 year relevant experience
Graduate/Post Graduate in Life Sciences or related field