Clinical Research Associate

medhunter.de

Hybrid
Ich-gcp and country regulations compliance
Site management and monitoring activities
Fluent in local languages and english
The role is accountable for performance and compliance for assigned protocols and sites in a country under the oversight of the CRA-Manager

Job Summary

  • The role is accountable for performance and compliance for assigned protocols and sites in a country under the oversight of the CRA-Manager.
  • The incumbent acts as the primary site contact and manager throughout all phases of a clinical research study, ensuring data accuracy and subject safety.
  • Candidates must possess proven skills in site management including patient recruitment and demonstrate high-level monitoring skills with independent professional judgment.

Matching Summary

The role is accountable for performance and compliance for assigned protocols and sites in a country under the oversight of the CRA-Manager.

Skills & Requirements

Must-have

  • ICH-GCP and country regulations compliance
  • Site management and monitoring activities
  • Fluent in local languages and English
  • Good Documentation Practices knowledge
  • Root cause analysis and corrective actions

Nice-to-have

  • Subject Matter Expertise in monitoring processes
  • Strong interpersonal and conflict management skills
  • Experience with audit and inspection support
  • Ability to work in a matrix multicultural environment
  • Growth mindset and self-driven approach

Key Requirements

  • Associate's degree plus 5 years healthcare experience or Bachelor's degree
  • At least 2 years direct site management (monitoring) experience
  • Valid driving license required for travel

Work Rights

Not specified

Tailored Resume

Cover Letter