Senior Analytical Monitor

Johnson & Johnson Innovative Medicine

High Wycombe, Buckinghamshire, United Kingdom
Hybrid (3 days onsite weekly)
Analytical risk based monitoring
Data analysis methods and processes
Site and subject level reviews
The job posting is for a Senior Analytical Monitor at Johnson & Johnson Innovative Medicine in High Wycombe, UK. The role involves overseeing clinical trial data analytics, ensuring compliance with regulatory guidelines, and collaborating with various stakeholders to enhance site performance

Job Summary

  • Empowered by technology, optimized processes and targeted data analytics, Analytical Monitors will enable Site Managers to dedicate a greater proportion of their time for meaningful engagement with sites, driving improved performance, data reliability and site satisfaction.
  • The Senior Analytical Monitor is accountable for executing processes and activities for multiple clinical trials in conformance to all relevant laws, regulations, guidelines, policies, and procedures.
  • We offer a competitive salary and extensive benefits package, a flexible working environment as we value work-life balance, and career development opportunities for those who want to grow and be part of our organisation.

Matching Summary

Match Score: 85

The job posting is for a Senior Analytical Monitor at Johnson & Johnson Innovative Medicine in High Wycombe, UK. The role involves overseeing clinical trial data analytics, ensuring compliance with regulatory guidelines, and collaborating with various stakeholders to enhance site performance.

Skills & Requirements

Must-have

  • Analytical Risk Based Monitoring
  • data analysis methods and processes
  • site and subject level reviews
  • identify potential risks
  • clinical trial execution

Nice-to-have

  • innovation and process improvement
  • cross-functional stakeholder influence
  • collaboration with external service providers
  • flexible working environment
  • career development opportunities

Key Requirements

  • Bachelor's degree or equivalent professional experience
  • 8-12 years of experience in Pharmaceutical, CRO or Biotech
  • Knowledge of trial site operations
  • Strong knowledge of regulatory guidelines (ICH-GCP)
  • Experience with data visualization tools
  • Project, Issue, and risk management experience
  • Experience working with technology platforms and systems
  • Experience working in highly diverse teams
  • Planning and coordination skills
  • Ability to influence stakeholders

Work Rights

Not specified

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