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Clinical Trial Assistant (CTA)(m/w/x)
Assisting with clinical trial design and analysis, interpreting complex medical data at a global clinical research organization. Bachelor's degree in scientific or healthcare field required. Global Employee Assistance Programme.
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
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
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
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
Not a perfect match?
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Clinical Trial Assistant (CTA)(m/w/x)
Assisting with clinical trial design and analysis, interpreting complex medical data at a global clinical research organization. Bachelor's degree in scientific or healthcare field required. Global Employee Assistance Programme.
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
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
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
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.
Not a perfect match?
- ICON plc
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Administrative Assistant im Bereich Legal & Compliance(m/w/x)
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Senior Clinical Trial Manager(m/w/x)
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