Central Monitoring Manager

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

📋 Description

• Lead and oversee initial and ongoing study Risk Management

• Engage in the selection and configuration of the RBM platform

• Conduct Centralized Monitoring for a study, which includes reviewing Key Risk Indicators, Statistical Analyses, and Quality Tolerance Limits

• Present 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 SDV and monitoring strategies for a study

• Organize and oversee Central Data Review activities within a study

• Contribute to Proposals and bid defense meetings by providing insights regarding Risk Based Monitoring services

• Relay study challenges to the Clinical Data Science team and collaborate on data-driven solutions

⛳️ Requirements

• Bachelor's degree or an equivalent combination of education, training, and experience

• Experience as a Clinical Study Lead/Manager

• Excellent communication and presentation abilities

• Strong leadership qualities and the capability to work autonomously

• Proficient critical thinking and analytical skills

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

• Flexibility to adapt to changing situations and learn rapidly

• Familiarity with the processes and functions involved in clinical trials

• Capability to understand the protocol and associated study risks

• Full working proficiency in English (German proficiency is advantageous)

• Proficient in MS Office applications

• Strong skills in Excel

🏝️ Benefits

• Excellent and flexible working conditions

• A distinctive blend of team collaboration and independent work

• Competitive salary and benefits package

• Comprehensive onboarding and mentorship program