Part-time Cra Ii - Klinischer Monitor (0.8 Fte) (m/w/d)

PPD (Thermo Fisher)

Munich, Germany
Not specified; not specified; not specified
Hybrid
2+ years clinical research monitor experience
Valid driver's license required
Fluency in english and german c1 level
The role involves performing and coordinating all aspects of clinical monitoring and site management to ensure trial compliance with ICH-GCP guidelines

Job Summary

  • The role involves performing and coordinating all aspects of clinical monitoring and site management to ensure trial compliance with ICH-GCP guidelines.
  • Candidates will conduct remote or on-site visits to assess protocol adherence, manage documentation, and perform risk-based monitoring activities.
  • This position offers a permanent part-time opportunity (0.8 FTE) with flexible work arrangements including home-based, office-based in Munich or Karlsruhe, or hybrid options.

Matching Summary

The role involves performing and coordinating all aspects of clinical monitoring and site management to ensure trial compliance with ICH-GCP guidelines.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • 2+ years clinical research monitor experience
  • Valid driver's license required
  • Fluency in English and German C1 level
  • Risk-based monitoring approach application
  • ICH-GCP guidelines knowledge
  • Travel up to 50-75% availability

Nice-to-have

  • Critical thinking and root cause analysis skills
  • Collaborative relationship building with sites
  • Experience with Clinical Trial Management Systems
  • Strong written business communication standards
  • Ability to work independently or in a team

Key Requirements

  • Bachelor's degree in life sciences
  • Full Right to work in Germany
  • Minimum 2 years as a clinical research monitor
  • Valid driver's license
  • German language fluency at C1 level

Work Rights

Full Right to work in Germany required

Tailored Resume

Cover Letter