Cra I/cra Ii (m/f/d) - Fsp Germany

PPD (Thermo Fisher) UK

Germany
Not specified; competitive salary mentioned; exten...
Hybrid
1+ years independent monitoring experience
Valid driver's license in germany
Fluency in german and english c1 level
This role involves managing clinical trial sites across Germany to ensure studies are conducted in full compliance with protocols and regulations

Job Summary

  • This role involves managing clinical trial sites across Germany to ensure studies are conducted in full compliance with protocols and regulations.
  • Candidates will perform on-site and remote monitoring activities using a risk-based approach while maintaining audit readiness at all assigned sites.
  • The position offers permanent employment with flexible working models, strong collaboration opportunities, and clear development pathways within a global organization.

Matching Summary

This role involves managing clinical trial sites across Germany to ensure studies are conducted in full compliance with protocols and regulations.

Salary

Not specified; Competitive salary mentioned; Extensive benefits package based on health and well-being

Skills & Requirements

Must-have

  • 1+ years independent monitoring experience
  • Valid driver's license in Germany
  • Fluency in German and English C1 level
  • Risk-based monitoring approach expertise
  • ICH-GCP and regulatory compliance knowledge

Nice-to-have

  • Strong critical thinking and problem-solving skills
  • Experience with root cause analysis and CAPA
  • Ability to work autonomously in dynamic environment
  • Mentoring activities and process improvement support
  • Collaborative team player with cross-functional focus

Key Requirements

  • Bachelor's degree in life sciences or equivalent
  • Minimum 1 year of CRA/monitor experience
  • Full right to work in Germany
  • Valid driver's license required
  • German and English fluency (C1 level)

Work Rights

Full right to work in Germany required

Tailored Resume

Cover Letter