Analyst Ii, Analytical Monitoring

J&J FAMILY OF COMPANIES

High Wycombe, United Kingdom
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Analytical risk based monitoring practices
Clinical trial site monitoring
Data analysis and reporting
** Johnson & Johnson is seeking an Analyst II for Analytical Monitoring in High Wycombe, UK, to support clinical trials with data analytics and monitoring practices. The ideal candidate will have a background in health sciences or data sciences, strong analytical skills, and experience in pharmaceutical or biotech industries. **

Job Summary

  • Johnson & Johnson provides an inclusive work environment where each person is considered as an individual and respects the diversity and dignity of employees.
  • The Analyst II Analytical Monitor supports multiple clinical trials by conducting analytical monitoring activities to detect issues early and improve site performance and data reliability.
  • The company offers a competitive salary, extensive benefits, flexible working environment, and career development opportunities.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking an Analyst II for Analytical Monitoring in High Wycombe, UK, to support clinical trials with data analytics and monitoring practices. The ideal candidate will have a background in health sciences or data sciences, strong analytical skills, and experience in pharmaceutical or biotech industries. **

Skills & Requirements

Must-have

  • Analytical Risk Based Monitoring practices
  • Clinical trial site monitoring
  • Data analysis and reporting
  • Cross-functional collaboration
  • Regulatory compliance with ICH-GCP
  • Use of clinical data management systems

Nice-to-have

  • Process improvement and innovation projects
  • Statistical analysis and data visualization
  • Knowledge of Risk-Based Quality Management
  • Experience with external clinical data sources
  • Strong written and verbal communication skills

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)
  • Project, issue, and risk management experience
  • Ability to communicate effectively in English

Work Rights

Not specified

Tailored Resume

Cover Letter