Analytical Monitor

ICON Clinical Research, LP

Mexico
Not specified; not specified; competitive benefits...
Fully remote
Centralized review methodologies
Ich gcp and fda regulations knowledge
Cross-functional team leadership
ICON Clinical Research is seeking an Analytical Monitor to lead and oversee centralized review activities for clinical trials in a fully remote capacity. The ideal candidate should possess strong leadership skills, extensive experience in clinical research, and a solid understanding of regulatory requirements

Job Summary

  • The role involves leading and overseeing the planning, execution, and monitoring of centralized review activities for clinical trials.
  • ICON offers a competitive salary along with health insurance, retirement planning, and a global Employee Assistance Programme.
  • Candidates must have extensive experience in clinical research or data management within the pharmaceutical or CRO industry.

Matching Summary

Match Score: 85

ICON Clinical Research is seeking an Analytical Monitor to lead and oversee centralized review activities for clinical trials in a fully remote capacity. The ideal candidate should possess strong leadership skills, extensive experience in clinical research, and a solid understanding of regulatory requirements.

Salary

Not specified; Not specified; Competitive benefits including health insurance and retirement planning

Skills & Requirements

Must-have

  • Centralized review methodologies
  • ICH GCP and FDA regulations knowledge
  • Cross-functional team leadership

Nice-to-have

  • Strong problem-solving abilities
  • Inclusive environment experience
  • Continuous improvement mindset

Key Requirements

  • Bachelor's or advanced degree in Life Sciences
  • Extensive experience in clinical research or data management
  • Knowledge of ICH GCP and FDA regulations

Work Rights

Not specified

Tailored Resume

Cover Letter