Analyst Ii, Analytical Monitoring

Johnson & Johnson MedTech

High Wycombe, Buckinghamshire, United Kingdom
3 days onsite
Analytical risk based monitoring practices
Clinical trial site monitoring
Data analysis and reporting tools
Johnson & Johnson MedTech is seeking an Analyst II for Analytical Monitoring in High Wycombe, UK, who will support clinical trial processes through data analytics and monitoring practices. The role requires strong analytical skills, knowledge of clinical trials, and collaboration with various stakeholders

Job Summary

  • Analyst II Analytical Monitors support execution of processes and activities for multiple clinical trials in conformance to all relevant laws, regulations, guidelines, policies, and procedures.
  • Empowered by technology, optimized processes and targeted data analytics, Analytical Monitors enable Site Managers to dedicate more time to meaningful engagement with sites, improving performance and data reliability.
  • Johnson & Johnson offers a competitive salary and extensive benefits package with a flexible working environment valuing work-life balance and career development opportunities.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking an Analyst II for Analytical Monitoring in High Wycombe, UK, who will support clinical trial processes through data analytics and monitoring practices. The role requires strong analytical skills, knowledge of clinical trials, and collaboration with various stakeholders.

Skills & Requirements

Must-have

  • Analytical Risk Based Monitoring practices
  • Clinical trial site monitoring
  • Data analysis and reporting tools
  • Cross-functional collaboration
  • Regulatory compliance with ICH-GCP
  • Project and risk management

Nice-to-have

  • Advanced analytics and biostatistics
  • Experience with complex data structures
  • Knowledge of Risk-based Quality Management
  • Process improvement and innovation
  • Strong communication skills
  • Hybrid work environment

Key Requirements

  • Bachelor's degree or equivalent experience
  • Approximately 4+ years pharmaceutical or biotech experience
  • Knowledge of clinical drug development processes
  • Working knowledge of regulatory guidelines (ICH-GCP)
  • Experience with project, issue, and risk management
  • Good written and verbal English communication skills

Work Rights

Not specified

Tailored Resume

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