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Expert Clinical Data Management(m/w/x)
Description
You will drive the integrity of clinical trials by managing complex data systems and collaborating with experts to ensure seamless data cleaning, reporting, and statistical evaluation.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Master’s degree in life sciences or equivalent qualification
- •Experience as technical writer or equivalent
- •Preferred experience with IVD and MD regulations
- •Optional experience with MD or IVD trials
- •Optional experience in validation
- •Effective verbal and written English communication
- •Independent and reliable project management skills
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Establish data management processes for clinical trials
- •Select and set up appropriate EDC systems
- •Develop non-EDC based data transfer tools
- •Create and review trial-specific Case Report Forms
- •Collaborate with project managers and statisticians
- •Perform data cleaning and statistical spot checks
- •Support interim analyses and trial closures
- •Configure and test electronic data capture databases
- •Migrate data according to internal procedures
- •Attend 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
Languages
English – Business Fluent
Benefits
Flexible Working
- •Hybrid work
Other Benefits
- •Attractive social benefits
Informal Culture
- •Inclusive work environment
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Expert Clinical Data Management(m/w/x)
The AI Job Search Engine
Description
You will drive the integrity of clinical trials by managing complex data systems and collaborating with experts to ensure seamless data cleaning, reporting, and statistical evaluation.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Master’s degree in life sciences or equivalent qualification
- •Experience as technical writer or equivalent
- •Preferred experience with IVD and MD regulations
- •Optional experience with MD or IVD trials
- •Optional experience in validation
- •Effective verbal and written English communication
- •Independent and reliable project management skills
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Establish data management processes for clinical trials
- •Select and set up appropriate EDC systems
- •Develop non-EDC based data transfer tools
- •Create and review trial-specific Case Report Forms
- •Collaborate with project managers and statisticians
- •Perform data cleaning and statistical spot checks
- •Support interim analyses and trial closures
- •Configure and test electronic data capture databases
- •Migrate data according to internal procedures
- •Attend 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
Languages
English – Business Fluent
Benefits
Flexible Working
- •Hybrid work
Other Benefits
- •Attractive social benefits
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.
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