Associate Clinical Research Associate

med-in.at

Hybrid
Fluent in local languages and english
Knowledge of ich-gcp and local laws
Hands-on good documentation practices
The role involves acting as the primary site contact and manager throughout all phases of a clinical research study

Job Summary

  • The role involves acting as the primary site contact and manager throughout all phases of a clinical research study.
  • Candidates must ensure data accuracy, protect subject rights, and maintain compliance with ICH-GCP and local regulations.
  • The position requires collaboration with various functional areas including regulatory affairs, pharmacovigilance, and legal teams.

Matching Summary

The role involves acting as the primary site contact and manager throughout all phases of a clinical research study.

Skills & Requirements

Must-have

  • Fluent in local languages and English
  • Knowledge of ICH-GCP and local laws
  • Hands-on Good Documentation Practices
  • Experience with CTMS and eTMF systems
  • Ability to perform root cause analysis

Nice-to-have

  • Strong interpersonal and conflict management skills
  • Growth mindset and self-driven approach
  • Experience in matrix multicultural environments
  • Solution-oriented problem solving
  • Commitment to customer focus

Key Requirements

  • Associate's degree + 3 years healthcare experience OR Bachelor's + 6 months experience
  • Bachelor's degree in non-scientific field + 2 years healthcare experience
  • Valid driving license required for site visits

Work Rights

Not specified

Tailored Resume

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