Job Summary

• ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
• The Central Monitor role involves implementing centralized monitoring strategies, performing risk assessments, generating reports, and collaborating with cross-functional teams to enhance clinical trial oversight.
• ICON offers competitive salaries and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

Skills & Requirements

Key Requirements

• ≥ 5 years pharmaceutical industry experience
• ≥ 3 years central monitoring or data analytics
• strong clinical trial development knowledge
• expertise in GCP/ICH and regulatory standards
• experience with e-databases and analytics systems
• project management experience
• experience in clinical research or CROs

Work Rights