Clinical Research Associate 2 (m/w/d), Iqvia Biotech, Based In Austria

IQVIA UK

Vienna, Austria
Base: starting at 4.000 eur; bonus/equity: not spe...
Site selection and monitoring
Gcp and ich guidelines
Subject recruitment plan development
Perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan

Job Summary

  • Perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan.
  • Evaluate the quality and integrity of site practices in accordance with regulatory requirements like GCP and ICH guidelines.
  • Enjoy the stability and resources of a leading, global contract research organization with intentional career growth and professional development.

Matching Summary

Perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan.

Salary

Base: starting at 4.000 EUR; Bonus/Equity: Not specified; Benefits: Company car, accident insurance, and more

Skills & Requirements

Must-have

  • site selection and monitoring
  • GCP and ICH guidelines
  • subject recruitment plan development
  • regulatory submission tracking
  • collaboration with site experts

Nice-to-have

  • mentoring less experienced team members
  • subject matter expert support
  • fast-paced environment adaptability

Key Requirements

  • Minimum two years on-site monitoring experience
  • University degree in life science or scientific discipline
  • Fluency in German (C1 level)
  • Good command of English
  • Driver's license class B

Work Rights

Not specified

Tailored Resume

Cover Letter