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Clinical Trial Assistant (CTA)(m/w/x)
Description
You will drive medical innovation by managing essential trial documentation and coordinating with cross-functional teams to ensure every clinical study meets strict regulatory standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Bachelor's degree in scientific or healthcare-related field
- •Experience or strong interest in clinical research
- •Knowledge of clinical trial processes and regulations
- •Excellent organizational and communication skills
- •Collaborative work style and attention to detail
- •Fluency in German and English
- •Residence in the Hamburg area
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Assist with clinical trial design and analysis
- •Interpret complex medical data
- •Coordinate and administer clinical trials
- •Ensure compliance with protocols and regulatory requirements
- •Maintain and organize clinical trial documentation
- •Manage study files and regulatory submissions
- •Prepare informed consent and case report forms
- •Collaborate with cross-functional teams
- •Track and report clinical trial metrics and milestones
Languages
German – Business Fluent
English – Business Fluent
Benefits
Healthcare & Fitness
- •Health insurance offerings
- •Health assessments
Retirement Plans
- •Competitive retirement planning
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
Childcare
- •Childcare vouchers
Company Bike
- •Bike purchase schemes
Corporate Discounts
- •Discounted gym memberships
Public Transport Subsidies
- •Subsidised travel passes
- zeroPRAXENFull-time/Part-timeWith HomeofficeNot specifiedMannheim
- SGS
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Clinical Trial Assistant (CTA)(m/w/x)
The AI Job Search Engine
Description
You will drive medical innovation by managing essential trial documentation and coordinating with cross-functional teams to ensure every clinical study meets strict regulatory standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Bachelor's degree in scientific or healthcare-related field
- •Experience or strong interest in clinical research
- •Knowledge of clinical trial processes and regulations
- •Excellent organizational and communication skills
- •Collaborative work style and attention to detail
- •Fluency in German and English
- •Residence in the Hamburg area
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Assist with clinical trial design and analysis
- •Interpret complex medical data
- •Coordinate and administer clinical trials
- •Ensure compliance with protocols and regulatory requirements
- •Maintain and organize clinical trial documentation
- •Manage study files and regulatory submissions
- •Prepare informed consent and case report forms
- •Collaborate with cross-functional teams
- •Track and report clinical trial metrics and milestones
Languages
German – Business Fluent
English – Business Fluent
Benefits
Healthcare & Fitness
- •Health insurance offerings
- •Health assessments
Retirement Plans
- •Competitive retirement planning
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
Childcare
- •Childcare vouchers
Company Bike
- •Bike purchase schemes
Corporate Discounts
- •Discounted gym memberships
Public Transport Subsidies
- •Subsidised travel passes
About the Company
ICON Clinical Research Germany GmbH
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
- zeroPRAXEN
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