Clinical Trial Coordinator Ii (m/f/d)

Thermo Fisher Scientific UK

Not specified; competitive salary mentioned; exten...
University degree in life sciences
Excellent english and german c1 level
Knowledge of ich good clinical practices
The role involves providing administrative and technical support to ensure audit readiness and high-quality data review for global clinical trials

Job Summary

  • The role involves providing administrative and technical support to ensure audit readiness and high-quality data review for global clinical trials.
  • Candidates will coordinate study activities, manage Investigator Site Files, and support RBM activities while maintaining strict adherence to regulations.
  • The position offers a stable career path within a well-established organization with flexible working models and an award-winning learning program.

Matching Summary

The role involves providing administrative and technical support to ensure audit readiness and high-quality data review for global clinical trials.

Salary

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

Skills & Requirements

Must-have

  • University degree in life sciences
  • Excellent English and German C1 level
  • Knowledge of ICH Good Clinical Practices
  • Proficiency in MS Office and clinical databases
  • Ability to handle multiple tasks efficiently

Nice-to-have

  • Strong customer focus and interpersonal skills
  • Self-motivated with a positive attitude
  • Experience with GoBalto and eTMF systems
  • Flexible to reprioritize workload
  • Team collaboration experience

Key Requirements

  • University degree in life sciences or equivalent
  • German language proficiency at C1 level
  • Knowledge of Country Regulations and SOPs
  • Completion of PPD clinical training program

Work Rights

Not specified

Tailored Resume

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