Cra Ii Or Senior Cra

ICON plc

Melbourne, Victoria, Australia
Not specified; competitive salary mentioned; vario...
Fully remote
Extensive cra experience in australia
Valid driver's license required
Ability to travel 60% of time
You will partner with a premier Biopharmaceutical company to monitor clinical trial sites ensuring adherence to protocols and GCP standards

Job Summary

  • You will partner with a premier Biopharmaceutical company to monitor clinical trial sites ensuring adherence to protocols and GCP standards.
  • The role involves conducting site visits, resolving issues, and providing training to maintain high standards of clinical trial conduct.
  • ICON offers competitive benefits including health insurance, retirement planning, and a global Employee Assistance Programme focused on well-being.

Matching Summary

You will partner with a premier Biopharmaceutical company to monitor clinical trial sites ensuring adherence to protocols and GCP standards.

Salary

Not specified; Competitive salary mentioned; Various annual leave entitlements and health insurance included

Skills & Requirements

Must-have

  • Extensive CRA experience in Australia
  • Valid driver's license required
  • Ability to travel 60% of time
  • Proficiency in clinical trial software
  • Strong understanding of GCP standards

Nice-to-have

  • Experience with cross-functional teams
  • Ability to train site staff and CRAs
  • Excellent communication skills
  • Proven problem-solving abilities

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate in Australia
  • Valid driver's license
  • Travel availability of at least 60%

Work Rights

Not specified

Tailored Resume

Cover Letter