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.