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 and evaluate their quality and integrity as per protocol, SOPs, respective regulations, and guidelines.
Facilitate early identification of site-level risk/issue(s) occurring during study conduct 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 systems proficiency
Czech and Slovak language proficiency
ICH-Good Clinical Practice knowledge
Nice-to-have
Results and detail-oriented approach
Strong telecommunication skills
Problem-solving skills
Attention to detail and accuracy
Key Requirements
2 to 5 years of work experience
Minimum 1 year relevant experience
Graduate/Post Graduate in Life Sciences or related field