Clinical Site Manager Ii

ICON

China
Not specified; competitive within country; + benef...
Extensive experience as clinical research associate
Strong understanding of clinical trial processes
Expertise in good clinical practice standards
The role involves leading clinical trial monitoring tasks with a focus on quality and continuous improvement

Job Summary

  • The role involves leading clinical trial monitoring tasks with a focus on quality and continuous improvement.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a commitment to an inclusive culture.
  • Candidates must have a Bachelor's degree in a scientific or healthcare field and extensive experience managing clinical trials.

Matching Summary

The role involves leading clinical trial monitoring tasks with a focus on quality and continuous improvement.

Salary

Not specified; Competitive within country; Additional benefits included

Skills & Requirements

Must-have

  • Extensive experience as Clinical Research Associate
  • Strong understanding of clinical trial processes
  • Expertise in Good Clinical Practice standards
  • Proficiency in clinical trial software tools
  • Willingness to travel approximately 60%

Nice-to-have

  • Ability to influence compliance in complex environments
  • Experience guiding other CRAs
  • Strong stakeholder management skills
  • Proven ability to manage multiple sites simultaneously

Key Requirements

  • Bachelor's degree in relevant scientific discipline
  • Extensive CRA experience
  • Knowledge of regulatory requirements and GCP

Work Rights

Not specified

Tailored Resume

Cover Letter