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Central Monitoring Manager(m/w/x)
Centralized monitoring and risk indicator review for clinical trials at a 30-year-old CRO. Centralized monitoring experience a plus. Flexible working conditions, team collaboration.
Requirements
- College/University degree or equivalent education/training/experience
- Clinical Study Lead/Manager experience
- Strong communication and presentation skills
- Leadership and independent work ability
- Centralized Monitoring experience (plus)
- Critical thinking and analytical skills
- Ability to work with complex data and provide insights
- Adaptability and quick learning ability
- Knowledge of clinical trial processes and risks
- Full working proficiency in English
- German proficiency (plus)
- Proficiency in MS Office applications
- Excel skills
Tasks
- Lead risk-based monitoring implementation
- Facilitate initial and ongoing risk management
- Participate in RBM platform selection and setup
- Perform centralized monitoring and review key risk indicators
- Conduct statistical analyses and quality tolerance limit reviews
- Present monitoring analysis results to teams and clients
- Manage issues in a cross-functional environment
- Develop and review study-specific plans
- Set up targeted SDV and monitoring strategies
- Manage central data review activities
- Contribute to proposals and bid defense meetings
- Communicate study challenges to Clinical Data Science
- Work out data-driven solutions
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Native
- German – Basic
Tools & Technologies
- MS Office
- Excel
Benefits
Competitive Pay
- Competitive salary package
Other Benefits
- Competitive benefits package
- Excellent working conditions
Flexible Working
- Flexible working conditions
Informal Culture
- Team collaboration
Purpose-Driven Work
- Independent work
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Central Monitoring Manager(m/w/x)
Centralized monitoring and risk indicator review for clinical trials at a 30-year-old CRO. Centralized monitoring experience a plus. Flexible working conditions, team collaboration.
Requirements
- College/University degree or equivalent education/training/experience
- Clinical Study Lead/Manager experience
- Strong communication and presentation skills
- Leadership and independent work ability
- Centralized Monitoring experience (plus)
- Critical thinking and analytical skills
- Ability to work with complex data and provide insights
- Adaptability and quick learning ability
- Knowledge of clinical trial processes and risks
- Full working proficiency in English
- German proficiency (plus)
- Proficiency in MS Office applications
- Excel skills
Tasks
- Lead risk-based monitoring implementation
- Facilitate initial and ongoing risk management
- Participate in RBM platform selection and setup
- Perform centralized monitoring and review key risk indicators
- Conduct statistical analyses and quality tolerance limit reviews
- Present monitoring analysis results to teams and clients
- Manage issues in a cross-functional environment
- Develop and review study-specific plans
- Set up targeted SDV and monitoring strategies
- Manage central data review activities
- Contribute to proposals and bid defense meetings
- Communicate study challenges to Clinical Data Science
- Work out data-driven solutions
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Native
- German – Basic
Tools & Technologies
- MS Office
- Excel
Benefits
Competitive Pay
- Competitive salary package
Other Benefits
- Competitive benefits package
- Excellent working conditions
Flexible Working
- Flexible working conditions
Informal Culture
- Team collaboration
Purpose-Driven Work
- Independent work
About the Company
PSI CRO
Industry
Pharmaceuticals
Description
The company is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation.
Not a perfect match?
- Immatics Biotechnologies GmbH
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