Central Monitoring Manager

This is a fully remote position, open to applicants in Spain.

📋 Description

• Lead and manage the initial and ongoing aspects of Risk Management for studies.

• Engage in the selection and implementation of the Risk-Based Monitoring (RBM) platform.

• Conduct Centralized Monitoring for studies, including the evaluation of Key Risk Indicators, Statistical Analyses, and Quality Tolerance Limits.

• Present findings from Centralized Monitoring analyses to study teams and clients while addressing issues in a cross-functional setting.

• Develop and assess study-specific plans.

• Establish and oversee targeted Source Data Verification (SDV) and monitoring strategies for studies.

• Set up and manage Central Data Review activities within a study.

• Contribute to proposals and bid defense meetings by providing insights into Risk-Based Monitoring services.

• Communicate study-related challenges to the Clinical Data Science group and collaborate on data-driven solutions.

⛳️ Requirements

• A College/University degree or an equivalent combination of education, training, and experience.

• Experience as a Clinical Study Lead/Manager.

• Excellent communication and presentation skills are crucial.

• Strong leadership abilities and the capacity to work independently are essential.

• Experience with Centralized Monitoring is advantageous.

• Strong critical thinking and analytical skills.

• Ability to work with complex data and offer insights into risk reports and trends.

• Flexibility to adapt to changing circumstances and a quick learning ability.

• Knowledge of clinical trial processes and functions, with an understanding of protocols and associated study risks.

• Full working proficiency in English (Spanish proficiency is an added advantage).

• Proficiency in MS Office applications, with strong Excel skills.

🏝️ Benefits

• Employees have the option to work remotely.