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

Make the right call and take your career to a whole new level.  Join the company that focuses on its people and invests in their professional development and success.