Clinical Monitoring (all genders)
Greiner AGUpper Austria, Austria
Posted January 24, 2026
59781.96 - 59781.96 EUR
Full Time
About the Company
Modern and collegial working environment with opportunities for professional growth.
Job Description
Collaborate with a clinical project team to conduct IVD/MD trials, perform site initiations, monitoring visits, and close-out visits. Ensure accuracy and completeness of study data and support trials submission to authorities.
Requirements
- University degree in biology, medicine, pharmacy or equivalent combination of education and experience
- At least 2 years of experience as a clinical monitor (CRA) in a CRO/medical device or pharmaceutical company
- Good knowledge of current industry practices related to the conduct of clinical studies (ICH-GCP, ISO 14155, ISO 20916)
- Good knowledge of MDR and IVDR and a good understanding of GDPR
- Excellent communication skills in business fluent German and good written and spoken English skills
Benefits
- Competitive salary with overpayment possible
- Flexible working environment (remote or in-office in Kremsmünster)
- Modern and collegial working environment
