Central Monitoring Manager

With the industry moving forward, the central monitoring function has become a top priority at PSI. We are looking for a person, who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.

You will:

• Lead and facilitate initial and ongoing study Risk Management • Participate in selection and setup of the RBM platform • Perform Centralized Monitoring for a study including review of Key Risk Indicators, Statistical Analyses and Quality Tolerance Limits • Present Centralized Monitoring analysis results to study teams and clients and manage issues in cross-functional environment • Develop and review study-specific Plans • Set up and manage targeted SDV and monitoring strategy for a study • Set up and manage Central Data Review activities in a study • Contribute to Proposals and bid defense meetings with information about Risk Based Monitoring services • Communicate study challenges to Clinical Data Science group and work out data-driven solutions • College/University degree or an equivalent combination of education, training and experience • Clinical Study Lead/Manager experience • Strong communication & presentation skills are essential • Leadership and ability to work independently are essential • Centralized Monitoring experience is a plus • Critical thinking and analytical skills • Ability to work with complex data and provide insight into risk reports and trends • Ability to adapt to changing circumstances and learn quickly • Knowledge of the process and functions in clinical trials, ability to understand the protocol and study associated risks • Full working proficiency in English (Estonian proficiency is a plus) • Proficiency in MS Office applications, Excel skills

This role is not only important for every CRO, but it is booming now. This is an opportunity to work on a frontline of the industry, set the grounds for risk-based models and get a global helicopter view on each project.