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Clinical Monitoring(m/w/x)
Monitoring IVD and MD studies, including site initiations and remote sessions, for a medical device manufacturer. Two years clinical monitor experience with ICH-GCP, ISO, MDR, IVDR, GDPR knowledge required. Flexible remote work options.
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
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- ICH-GCP
- ISO 14155
- ISO 20916
- MDR
- IVDR
- GDPR
- FDA regulations
- ISO regulations
- CLSI guidelines
Benefits
Flexible Working
- Remote work
Informal Culture
- Inclusive work environment
- Home
- Jobs in Austria
- Clinical MonitoringClinical Monitoring at Greiner Bio-One GmbH
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- Home
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- Clinical MonitoringClinical Monitoring at Greiner Bio-One GmbH
Clinical Monitoring(m/w/x)
Monitoring IVD and MD studies, including site initiations and remote sessions, for a medical device manufacturer. Two years clinical monitor experience with ICH-GCP, ISO, MDR, IVDR, GDPR knowledge required. Flexible remote work options.
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
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- ICH-GCP
- ISO 14155
- ISO 20916
- MDR
- IVDR
- GDPR
- FDA regulations
- ISO regulations
- CLSI guidelines
Benefits
Flexible Working
- Remote work
Informal Culture
- Inclusive work environment
About the Company
Greiner Bio-One GmbH
Industry
Healthcare
Description
Das Unternehmen Greiner Bio-One bietet einen Arbeitsplatz, an dem Team-Player und Visionäre in der Gesundheitsbranche Großes bewegen können.
Not a perfect match?
- Fronius International GmbH
Qualitätsplaner für Produktentwicklungsprojekte(m/w/x)
Full-timeWith HomeofficeExperiencedThalheim bei Wels - Unbekannt
Consultant - Monitoring global(m/w/x)
Full-timeWith HomeofficeNot specifiedAnsfelden, Wien, Salzburg, Bad Hall, Graz, Münchenfrom 52,000 / year - Fronius International GmbH
Mitarbeiter im Qualitätsmanagement für externe Industrialisierungsprojekte(m/w/x)
Full-timeWith HomeofficeExperiencedSattledt - TGW Logistics
Global Supplier Quality Engineer(m/w/x)
Full-timeWith HomeofficeExperiencedMarchtrenkfrom 48,412 / year - TGW Logistics
Customer Insights Manager:in(m/w/x)
Full-timeWith HomeofficeExperiencedMarchtrenkfrom 47,547 / year