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Clinical Trial Assistant(m/w/x)
Administrative coordination and medical data interpretation for global drug development studies. Bachelor's degree in a scientific or healthcare-related field required. Global employee assistance program and life assurance.
Requirements
- Bachelor's degree in scientific or healthcare-related field
- Prior experience or interest in clinical research
- Knowledge of clinical trial processes and regulations
- Excellent organizational and communication skills
- Collaborative work ability and attention to detail
Tasks
- Assist with clinical trial design and analysis
- Interpret complex medical data
- Contribute to innovative treatment and therapy advancement
- Coordinate and administer clinical trials
- Ensure compliance with protocols and regulatory requirements
- Maintain and organize clinical trial documentation
- Manage study files and essential documents
- Organize regulatory submissions
- Prepare informed consent and case report forms
- Facilitate communication across cross-functional teams
- Ensure smooth execution of clinical trials
- Track and report clinical trial metrics and milestones
Education
- Bachelor's degree
Languages
- 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?
- ICON plcFull-timeRemoteSeniorFrankfurt am Main
- IQVIA
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Experienced Clinical Trials Assistant(m/w/x)
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Study Start Up Associate I(m/w/x)
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Clinical Research Associate - Sponsor Dedicated(m/w/x)
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Clinical Trial Assistant(m/w/x)
Administrative coordination and medical data interpretation for global drug development studies. Bachelor's degree in a scientific or healthcare-related field required. Global employee assistance program and life assurance.
Requirements
- Bachelor's degree in scientific or healthcare-related field
- Prior experience or interest in clinical research
- Knowledge of clinical trial processes and regulations
- Excellent organizational and communication skills
- Collaborative work ability and attention to detail
Tasks
- Assist with clinical trial design and analysis
- Interpret complex medical data
- Contribute to innovative treatment and therapy advancement
- Coordinate and administer clinical trials
- Ensure compliance with protocols and regulatory requirements
- Maintain and organize clinical trial documentation
- Manage study files and essential documents
- Organize regulatory submissions
- Prepare informed consent and case report forms
- Facilitate communication across cross-functional teams
- Ensure smooth execution of clinical trials
- Track and report clinical trial metrics and milestones
Education
- Bachelor's degree
Languages
- 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 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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Experienced Clinical Trials Assistant(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main, Hamburg - ICON plc
Study Start Up Associate I(m/w/x)
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Clinical Research Associate - Sponsor Dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main