Clinical Research Associate 2 Or Senior Clinical Research Associate 1 (m/w/d), Single Sponsor

IQVIA

Frankfurt, Germany
Fully remote
Site selection and monitoring
Gcp and ich guidelines
Regulatory submissions tracking
Perform site selection, initiation, monitoring, and close-out visits, supporting recruitment and evaluating site quality against regulatory requirements

Job Summary

  • Perform site selection, initiation, monitoring, and close-out visits, supporting recruitment and evaluating site quality against regulatory requirements.
  • Manage study progress by tracking submissions, recruitment, CRF completion, and data query resolution, collaborating with site experts and client representatives.
  • Enjoy permanent employment, home-office flexibility, competitive salary, company car, and resources promoting career growth.

Matching Summary

Perform site selection, initiation, monitoring, and close-out visits, supporting recruitment and evaluating site quality against regulatory requirements.

Skills & Requirements

Must-have

  • site selection and monitoring
  • GCP and ICH guidelines
  • regulatory submissions tracking
  • English and German fluency

Nice-to-have

  • mentoring less experienced team members
  • subject matter expert
  • remote monitoring involvement

Key Requirements

  • 2-4 years on-site monitoring experience
  • University degree or apprenticeship in healthcare
  • Knowledge of GCP and ICH guidelines
  • C1 level German fluency
  • Valid driver's license class B

Work Rights

Not specified

Tailored Resume

Cover Letter