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GRGreiner Bio-One GmbH

Clinical Monitoring(m/w/x)

Kremsmünster
from 59,781.96 / year
Full-timeWith Home OfficeExperienced

You will drive the success of clinical trials by managing site monitoring and regulatory compliance, ensuring data integrity while acting as the vital link between trial sites and the sponsor.

Requirements

  • Degree in biology, medicine, pharmacy or equivalent
  • Two years experience as clinical monitor
  • Knowledge of ICH-GCP, ISO 14155, ISO 20916
  • Knowledge of MDR, IVDR and GDPR
  • Advantageous experience of FDA, ISO, CLSI
  • Independent and reliable work style
  • Excellent German and English communication skills
  • Willingness to travel

Tasks

  • Collaborate with clinical project teams to set objectives and timelines
  • Conduct IVD and MD studies following protocols and regulations
  • Perform feasibility assessments for trial sites
  • Execute site initiations and on-site monitoring visits
  • Monitor GBO labs and conduct remote monitoring sessions
  • Manage trial site close-out visits
  • Train study team members on protocol and local regulations
  • Ensure the accuracy and completeness of study data
  • Support international trial submissions to authorities and ethics committees
  • Act as the primary liaison between trial sites and sponsors
  • Create study-specific forms
  • Maintain the Trial Master File

Work Experience

2 years

Education

Bachelor's degree

Languages

GermanBusiness FluentEnglishBusiness Fluent

Tools & Technologies

ICH-GCPISO 14155ISO 20916MDRIVDRGDPRFDA regulationsISO regulationsCLSI guidelines

Benefits

Flexible Working

  • Remote work

Informal Culture

  • Inclusive work environment
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