Clinical Monitoring (all Genders)

Greiner AG

Kremsmünster, AT
Base: eur 59,781.96 minimum; bonus/equity: not spe...
On-site
Conduct ivd and md studies
Knowledge of iso 14155 and gcp
Understanding of mdr and ivdr regulations
The role involves collaborating with a clinical project team to establish objectives and timelines for IVD/MD trials

Job Summary

  • The role involves collaborating with a clinical project team to establish objectives and timelines for IVD/MD trials.
  • Candidates must ensure the accuracy, validity, and completeness of study data while supporting international trial submissions.
  • The position offers a minimum gross salary of EUR 59,781.96 based on the collective agreement for the chemical industry.

Matching Summary

The role involves collaborating with a clinical project team to establish objectives and timelines for IVD/MD trials.

Salary

Base: EUR 59,781.96 minimum; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Conduct IVD and MD studies
  • Knowledge of ISO 14155 and GCP
  • Understanding of MDR and IVDR regulations
  • Business fluent German language skills
  • Good written and spoken English skills

Nice-to-have

  • Experience with FDA and CLSI guidelines
  • Ability to work independently in fast-paced environment
  • Familiarity with TMF maintenance procedures

Key Requirements

  • University degree in biology, medicine, pharmacy or equivalent
  • At least 2 years of experience as a clinical monitor (CRA)
  • Good knowledge of GDPR and local regulations

Work Rights

Not specified

Tailored Resume

Cover Letter