Central Monitoring Manager

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

📋 Description

• Lead and oversee the initial and ongoing management of study risks.

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

• Conduct Centralized Monitoring for studies, including the assessment 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 evaluate study-specific plans.

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

• Organize and manage Central Data Review activities within a study.

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

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

⛳️ Requirements

• A college or university degree, or an equivalent combination of education, training, and experience.

• Experience as a Clinical Study Lead or Manager.

• Excellent communication and presentation abilities.

• Demonstrated leadership skills and the capacity to work independently.

• Strong critical thinking and analytical capabilities.

• Proficient in working with complex data and providing insights into risk reports and trends.

• Adaptable to changing circumstances and quick to learn.

• Familiarity with the processes and functions involved in clinical trials.

• Ability to comprehend the protocol and associated study risks.

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

• Proficient in Microsoft Office applications.

• Advanced Excel skills.

🏝️ Benefits

• Employees have the option to work remotely.