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.