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ICON

Shanghai, China
Clinical trial coordination and monitoring
Compliance with regulatory requirements
Study documentation management
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
  • The Clinical Research Associate will independently coordinate study setup and monitoring, manage documentation, resolve sponsor queries, and ensure compliance with protocols and regulations.
  • ICON offers competitive salary 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

ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • Clinical trial coordination and monitoring
  • Compliance with regulatory requirements
  • Study documentation management
  • Sponsor query resolution
  • Stakeholder relationship development
  • Patient safety assurance
  • Travel availability up to 60%

Nice-to-have

  • Excellent written and verbal communication
  • Good social skills for timely query handling
  • Inclusive and diverse work culture
  • Work-life balance focus
  • Collaborative team environment

Key Requirements

  • University degree in medicine or science
  • Knowledge of ICH-GCP guidelines
  • Ability to review and evaluate medical data
  • Excellent English communication skills
  • Valid driver’s license
  • Ability to travel at least 60% internationally and domestically

Work Rights

Not specified

Tailored Resume

Cover Letter