Principal Centralized Monitoring Analyst- Risk Manager
Thermo Fisher Scientific UK
8+ years clinical trial experience
Centralized monitoring expertise
Risk-based quality management methodology
This role serves as a lead subject matter expert responsible for developing complex tools to detect, investigate, and mitigate risks in clinical trials
Job Summary
This role serves as a lead subject matter expert responsible for developing complex tools to detect, investigate, and mitigate risks in clinical trials.
The successful candidate will independently lead the design of centralized monitoring plans, manage review timelines, and ensure high-quality delivery across multiple high-volume projects.
Joining Thermo Fisher Scientific offers the opportunity to work within a global team that values passion, innovation, and scientific excellence while making a real difference in organizational performance.
Matching Summary
This role serves as a lead subject matter expert responsible for developing complex tools to detect, investigate, and mitigate risks in clinical trials.
Skills & Requirements
Must-have
8+ years clinical trial experience
Centralized monitoring expertise
Risk-based quality management methodology
Complex data analysis and root cause investigation
Project leadership for study tools and plans
Nice-to-have
Cross-functional collaboration skills
Mentoring and training junior staff
Strong negotiation and communication abilities
Adaptability to changing situations
Experience with biostatistics and medical monitoring
Key Requirements
Bachelor's degree or equivalent qualification
Minimum 8 years of relevant experience
Knowledge of regulatory guidelines and global SOPs