Clinical Data Reviewer

You will join a widespread, yet closely-knit team with the same mentality and desire to develop smart and intelligent approach to project monitoring. You will help to shape the future of effective risk-based monitoring at PSI and ensure higher quality of study data. You will spend time monitoring study data remotely, identifying errors and issues with site performance.
You will:
Review clinical data remotely and identify errors, systemic issues and trends related to data integrity, participant safety and site performance
Generate, follow up and resolve data queries and site issues, and identify potential protocol deviations
Develop and maintain study-specific Central Data Review tools, templates and tracking materials
Support the setup and management of risk-based and central monitoring tools and activities
Assist with central monitoring signal review, root cause investigation and follow-up
Support the Central Monitoring Manager with study data, documents and reports
Contribute to inspection readiness, including eTMF QC and study archive activities
Bachelor’s degree
At least 1 year of experience in the Clinical Research Industry
Clinical Monitoring experience is an advantage
English proficiency at CEFR B2 level or above
Proficiency in MS Office applications
Analytical mindset and attention to detail
Ability to learn, plan and work effectively in a dynamic team environment

Employment type
Full-time

Work arrangement
No