Clinical Research Associate

beonemedicines.ae

Base: 44,800.00 eur - 56,000.00 eur; bonus/equity:...
Ich guidelines and gcp compliance
Oncology/hematology clinical trials
Site identification and selection
The CRA executes clinical monitoring activities at clinical trial sites in accordance with ICH guidelines, GCP, and local regulations

Job Summary

  • The CRA executes clinical monitoring activities at clinical trial sites in accordance with ICH guidelines, GCP, and local regulations.
  • Candidates must possess a BS in a relevant scientific discipline and a minimum of 2 years of monitoring experience.
  • The role requires fluency in both English and Italian to effectively collaborate with regional teams and clinical study sites.

Matching Summary

The CRA executes clinical monitoring activities at clinical trial sites in accordance with ICH guidelines, GCP, and local regulations.

Salary

Base: 44,800.00 EUR - 56,000.00 EUR; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • ICH guidelines and GCP compliance
  • Oncology/hematology clinical trials
  • Site identification and selection
  • Monitoring visit execution
  • Data query resolution

Nice-to-have

  • SSU experience preferred
  • Collaborative team spirit
  • Innovation mindset
  • Fluent in English and Italian
  • Passionate interest in fighting cancer

Key Requirements

  • BS in scientific discipline
  • Minimum 2 years CRA monitoring experience
  • Experience in oncology/hematology trials preferred
  • Fluency in English and Italian

Work Rights

Not specified

Tailored Resume

Cover Letter