Central Monitoring Manager

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

📋 Description

• Oversee and guide the initial and ongoing Risk Management for studies.

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

• Conduct Centralized Monitoring for a study, which includes the assessment of Key Risk Indicators, Statistical Analyses, and Quality Tolerance Limits.

• Deliver Centralized Monitoring analysis findings to study teams and clients.

• Address issues within a cross-functional setting.

• Create and evaluate study-specific Plans.

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

• Organize and oversee Central Data Review activities within studies.

• Contribute to Proposals and participate in bid defense discussions by providing insights on Risk-Based Monitoring services.

• Relay study 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 abilities.

• Strong leadership skills and the capability to work independently.

• Proficient in critical thinking and analytical reasoning.

• Competent in handling complex data and offering insights into risk reports and trends.

• Flexible in adapting to changing circumstances and quick to learn.

• Understanding of clinical trial processes and functions.

• Ability to comprehend study protocols and associated risks.

• Full working proficiency in English; proficiency in Lithuanian is an advantage.

• Skilled in MS Office applications.

• Proficient in Excel.

🏝️ Benefits

• Excellent working conditions.

• Comprehensive training opportunities.

• Supportive team environment.

• Potential for personal and professional development.

• Competitive salary and benefits package.