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Expert Clinical Data Management(m/w/x)
Setting up EDC systems and data transfer tools for clinical trials. Master's degree in life sciences or equivalent qualification required. Attractive social benefits, equal opportunities.
Requirements
- Master's degree in life sciences or equivalent qualification
- Technical writer experience for medical device/pharma company
- Preferred experience with IVD and MD regulatory landscape
- Preferred experience with MD/IVD trials
- Preferred experience in validation
- Effective verbal and written English communication
- Independent and reliable work management
- Ability to manage multiple project tasks and priorities
- Adaptability to fast-paced, changing international environment
Tasks
- Set up data management processes for clinical trials
- Select or create appropriate EDC systems and data transfer tools
- Create and review trial-specific (e)CRFs according to trial plans
- Collaborate with clinical project managers and statisticians for data cleaning and statistical evaluation
- Configure, migrate, and test EDC databases based on procedures and requirements
- Attend trial-specific team meetings and produce status reports
- Generate and close data queries
- Define interfaces between data management and existing processes
- Train colleagues in clinical data management
Work Experience
- approx. 1 - 4 years
Education
- Vocational certification
Languages
- English – Business Fluent
Benefits
Other Benefits
- Attractive social benefits
- Equal opportunities
Informal Culture
- Diversity as a strength
- Inclusive work environment
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Expert Clinical Data Management(m/w/x)
Setting up EDC systems and data transfer tools for clinical trials. Master's degree in life sciences or equivalent qualification required. Attractive social benefits, equal opportunities.
Requirements
- Master's degree in life sciences or equivalent qualification
- Technical writer experience for medical device/pharma company
- Preferred experience with IVD and MD regulatory landscape
- Preferred experience with MD/IVD trials
- Preferred experience in validation
- Effective verbal and written English communication
- Independent and reliable work management
- Ability to manage multiple project tasks and priorities
- Adaptability to fast-paced, changing international environment
Tasks
- Set up data management processes for clinical trials
- Select or create appropriate EDC systems and data transfer tools
- Create and review trial-specific (e)CRFs according to trial plans
- Collaborate with clinical project managers and statisticians for data cleaning and statistical evaluation
- Configure, migrate, and test EDC databases based on procedures and requirements
- Attend trial-specific team meetings and produce status reports
- Generate and close data queries
- Define interfaces between data management and existing processes
- Train colleagues in clinical data management
Work Experience
- approx. 1 - 4 years
Education
- Vocational certification
Languages
- English – Business Fluent
Benefits
Other Benefits
- Attractive social benefits
- Equal opportunities
Informal Culture
- Diversity as a strength
- 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?
- Greiner Bio-One GmbH
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