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CRA I (sponsor dedicated)(m/w/x)
Clinical study setup and monitoring, including documentation and query resolution, for a specific pharmaceutical client at a healthcare intelligence CRO. University degree in medicine or science, with ICH-GCP knowledge and 60% travel willingness required. Single-client focus with close collaboration.
Requirements
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines and medical data evaluation
- Excellent written and verbal English and German
- Good social skills and timely query management
- Willingness to travel 60% and valid drivers license
Tasks
- Coordinate all study setup and monitoring activities
- Complete accurate study status reports
- Maintain comprehensive study documentation
- Resolve sponsor-generated queries efficiently
- Manage study cost efficiency
- Prepare and review study documentation
- Conduct feasibility studies for new proposals
- Develop collaborative relationships with clinical investigators and site staff
- Ensure patient safety through protocol and regulatory compliance
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- ICH-GCP guidelines
Benefits
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
- Reasonable accommodations
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Informal Culture
- Inclusive and accessible environment
Not a perfect match?
- ICON plcFull-timeRemoteNot specifiedFrankfurt am Main
- ICON plc
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CRA I (sponsor dedicated)(m/w/x)
Clinical study setup and monitoring, including documentation and query resolution, for a specific pharmaceutical client at a healthcare intelligence CRO. University degree in medicine or science, with ICH-GCP knowledge and 60% travel willingness required. Single-client focus with close collaboration.
Requirements
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines and medical data evaluation
- Excellent written and verbal English and German
- Good social skills and timely query management
- Willingness to travel 60% and valid drivers license
Tasks
- Coordinate all study setup and monitoring activities
- Complete accurate study status reports
- Maintain comprehensive study documentation
- Resolve sponsor-generated queries efficiently
- Manage study cost efficiency
- Prepare and review study documentation
- Conduct feasibility studies for new proposals
- Develop collaborative relationships with clinical investigators and site staff
- Ensure patient safety through protocol and regulatory compliance
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- ICH-GCP guidelines
Benefits
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
- Reasonable accommodations
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Informal Culture
- Inclusive and accessible environment
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Not a perfect match?
- ICON plc
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