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Clinical Trial Associate(m/w/x)
Assisting with clinical trial coordination and documentation for a global CRO. Bachelor's degree and knowledge of trial processes required. Annual leave entitlements, health insurance, and retirement planning.
Requirements
- Bachelor's degree in scientific/healthcare field
- Clinical research experience or strong interest
- Knowledge of clinical trial processes, regulations, guidelines
- Excellent organizational and communication skills
- Collaborative work in fast-paced environment
- Attention to detail
- Willingness to travel approximately 10%
- Fluency in German and English language
Tasks
- Assist in clinical trial coordination and administration
- Ensure compliance with protocols and regulatory requirements
- Maintain and organize clinical trial documentation
- Prepare study-related materials like informed consent forms
- Support cross-functional team communication
- 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
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
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Clinical Trial Associate(m/w/x)
Assisting with clinical trial coordination and documentation for a global CRO. Bachelor's degree and knowledge of trial processes required. Annual leave entitlements, health insurance, and retirement planning.
Requirements
- Bachelor's degree in scientific/healthcare field
- Clinical research experience or strong interest
- Knowledge of clinical trial processes, regulations, guidelines
- Excellent organizational and communication skills
- Collaborative work in fast-paced environment
- Attention to detail
- Willingness to travel approximately 10%
- Fluency in German and English language
Tasks
- Assist in clinical trial coordination and administration
- Ensure compliance with protocols and regulatory requirements
- Maintain and organize clinical trial documentation
- Prepare study-related materials like informed consent forms
- Support cross-functional team communication
- 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
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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.
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