Associate Clinical Research Monitor (cra) (m/w/d) - Zunächst Befristet Auf 1 Jahr

Medtronic UK

Germany
Germany: 51,200.00 eur - 76,800.00 eur; bonus/equi...
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Gcp and regulatory requirements
Site management and monitoring
Patient safety focus
** Medtronic UK is seeking an Associate Clinical Research Monitor to oversee clinical trials in Germany, ensuring compliance with regulatory and ethical standards. The role requires a relevant degree and experience in clinical research monitoring, with responsibilities including collaboration with study centers and managing study documentation. **

Job Summary

  • As an Associate Clinical Research Monitor, you will directly contribute to the successful execution of clinical studies, ensuring compliance with study protocols, Good Clinical Practice (GCP), and all relevant regulatory requirements.
  • This role involves building and maintaining collaborations with investigators, clinical research organizations (CROs), and research institutions to initiate and advance clinical studies for innovative medical technologies.
  • Medtronic offers a competitive salary and flexible benefits package, recognizing employee contributions and supporting them at every career and life stage.

Matching Summary

Match Score: 75

** Medtronic UK is seeking an Associate Clinical Research Monitor to oversee clinical trials in Germany, ensuring compliance with regulatory and ethical standards. The role requires a relevant degree and experience in clinical research monitoring, with responsibilities including collaboration with study centers and managing study documentation. **

Salary

Germany: 51,200.00 EUR - 76,800.00 EUR; Bonus/Equity: Eligible for Medtronic Incentive Plan (MIP); Benefits: Competitive Benefits Package

Skills & Requirements

Must-have

  • GCP and regulatory requirements
  • Site management and monitoring
  • Patient safety focus
  • Collaboration with study centers
  • Proficiency in Word, PowerPoint, Excel

Nice-to-have

  • Life-long career exploration
  • Championing healthcare access
  • Breaking down innovation barriers

Key Requirements

  • Bachelor's, Master's, or Diploma in a science or health-related field
  • Proven experience in Clinical Research Monitoring
  • Understanding of GCP, ICH guidelines, FDA-CFR, ISO standards
  • Fluent German and English language skills

Work Rights

Not specified

Tailored Resume

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