Senior Cra/ Cra Ii

ICON Clinical Research, LP

Unknown, Unknown, Czech Republic
Not specified; competitive salary mentioned; vario...
Fully remote
Bachelor's degree in scientific discipline
Extensive clinical research associate experience
Strong understanding of regulatory requirements
The role involves leading clinical trial monitoring tasks with a focus on quality and continuous improvement while ensuring adherence to Good Clinical Practice standards

Job Summary

  • The role involves leading clinical trial monitoring tasks with a focus on quality and continuous improvement while ensuring adherence to Good Clinical Practice standards.
  • ICON offers a competitive salary along with various benefits including health insurance, retirement planning, and a global Employee Assistance Programme.
  • Candidates must have extensive experience managing multiple sites simultaneously and possess strong organizational skills to drive compliance within complex environments.

Matching Summary

The role involves leading clinical trial monitoring tasks with a focus on quality and continuous improvement while ensuring adherence to Good Clinical Practice standards.

Salary

Not specified; Competitive salary mentioned; Various annual leave entitlements; Health insurance offerings; Retirement planning offerings

Skills & Requirements

Must-have

  • Bachelor's degree in scientific discipline
  • Extensive Clinical Research Associate experience
  • Strong understanding of regulatory requirements
  • Proficiency in clinical trial software tools
  • Ability to travel approximately 60%

Nice-to-have

  • Experience guiding other CRAs
  • Excellent communication skills
  • Proven problem-solving abilities
  • Willingness to foster inclusive environment

Key Requirements

  • Bachelor's degree in relevant field
  • Extensive CRA experience required
  • Travel availability (approx. 60%)
  • Knowledge of GCP and regulations

Work Rights

Not specified

Tailored Resume

Cover Letter