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Clinical Research Associate (CRA)(m/w/x)
Monitoring clinical trials, including site selection and remote oversight, for a global lab group serving food, pharma, and consumer goods sectors. Minimum 2 years clinical monitoring experience required. Diverse project scope across food, pharma, and consumer goods.
Requirements
- Minimum 2 years of clinical monitoring experience
- Degree in scientific or medical discipline or equivalent
- Very good knowledge of Good Clinical Practice/ICH Guidelines
- Proven ability to work independently in a fast-paced environment
- Excellent communication, interpersonal, and organizational skills
- Fluency in German and high level of English language
Tasks
- Act as a liaison between the sponsor, CRO, and trial site
- Perform monitoring visits, including site selection, initiation, periodic, and close-out visits
- Conduct remote monitoring of clinical trials
- Generate and update monitoring plans and site initiation presentations
- Evaluate the quality and integrity of site practices
- Serve as a contact for clinical trial suppliers and assigned vendors
- Identify and escalate protocol deviations and data discrepancies
- Ensure compliance with clinical trial protocols and GCP/ICH guidelines
- Collaborate closely with various departments at bioskin and freelance CRAs
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
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Clinical Research Associate (CRA)(m/w/x)
Monitoring clinical trials, including site selection and remote oversight, for a global lab group serving food, pharma, and consumer goods sectors. Minimum 2 years clinical monitoring experience required. Diverse project scope across food, pharma, and consumer goods.
Requirements
- Minimum 2 years of clinical monitoring experience
- Degree in scientific or medical discipline or equivalent
- Very good knowledge of Good Clinical Practice/ICH Guidelines
- Proven ability to work independently in a fast-paced environment
- Excellent communication, interpersonal, and organizational skills
- Fluency in German and high level of English language
Tasks
- Act as a liaison between the sponsor, CRO, and trial site
- Perform monitoring visits, including site selection, initiation, periodic, and close-out visits
- Conduct remote monitoring of clinical trials
- Generate and update monitoring plans and site initiation presentations
- Evaluate the quality and integrity of site practices
- Serve as a contact for clinical trial suppliers and assigned vendors
- Identify and escalate protocol deviations and data discrepancies
- Ensure compliance with clinical trial protocols and GCP/ICH guidelines
- Collaborate closely with various departments at bioskin and freelance CRAs
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
About the Company
Eurofins
Industry
Healthcare
Description
Das Unternehmen ist die führende Labor-Gruppe weltweit für Analyse- und Serviceleistungen in der Lebensmittel-, Pharma-, Umwelt- und Konsumgüterindustrie.
Not a perfect match?
- DE10 AstraZeneca GmbH
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