ICON plc
Clinical Trial Assistant(m/w/x)
Full-timeRemoteExperienced
Frankfurt am Main
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ICICON plc
(Senior) Clinical Trial Assistant(m/w/x)
Frankfurt am Main
Full-timeRemoteExperienced
Nejo AI Summary
Supporting clinical trial management at a global CRO, handling documentation and coordinating meetings. Extensive clinical trial support experience required. 4 weeks vacation, health insurance, retirement planning.
Requirements
- Strong foundation in clinical trial management
- Ability to work independently and guide others
- Bachelor's degree in relevant scientific or healthcare field
- Extensive experience in clinical trial support
- Solid understanding of clinical trial processes
- Solid understanding of regulatory requirements
- Strong organizational skills
- Strong multitasking skills
- Ability to manage multiple tasks and projects effectively
- Proficiency in clinical trial management systems
- Proficiency in relevant software
- Keen eye for detail in documentation
- Keen eye for detail in data management
- Excellent communication skills
- Excellent interpersonal skills
- Excellent problem-solving skills
- Ability to work collaboratively with diverse teams
- Ability to work collaboratively with diverse stakeholders
- Willingness to travel as required
- Travel approximately 10%
- Encouraged to apply even if not all requirements met
Tasks
- Support clinical trial management
- Handle administrative tasks
- Manage clinical trial documentation
- Coordinate meetings
- Maintain trial-related records
- Prepare regulatory documents
- Submit regulatory documents
- Ensure compliance with study protocols
- Ensure regulatory compliance
- Collaborate with cross-functional teams
- Support trial operations
- Resolve trial issues
- Monitor trial progress
- Track trial progress
- Manage site communications
- Ensure timely delivery of study materials
- Build relationships with site staff
- Maintain relationships with stakeholders
- Facilitate smooth trial operations
- Support project success
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- clinical trial management systems
- relevant software
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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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ICICON plc
(Senior) Clinical Trial Assistant(m/w/x)
Frankfurt am Main
Full-timeRemoteExperienced
Nejo AI Summary
Supporting clinical trial management at a global CRO, handling documentation and coordinating meetings. Extensive clinical trial support experience required. 4 weeks vacation, health insurance, retirement planning.
Requirements
- Strong foundation in clinical trial management
- Ability to work independently and guide others
- Bachelor's degree in relevant scientific or healthcare field
- Extensive experience in clinical trial support
- Solid understanding of clinical trial processes
- Solid understanding of regulatory requirements
- Strong organizational skills
- Strong multitasking skills
- Ability to manage multiple tasks and projects effectively
- Proficiency in clinical trial management systems
- Proficiency in relevant software
- Keen eye for detail in documentation
- Keen eye for detail in data management
- Excellent communication skills
- Excellent interpersonal skills
- Excellent problem-solving skills
- Ability to work collaboratively with diverse teams
- Ability to work collaboratively with diverse stakeholders
- Willingness to travel as required
- Travel approximately 10%
- Encouraged to apply even if not all requirements met
Tasks
- Support clinical trial management
- Handle administrative tasks
- Manage clinical trial documentation
- Coordinate meetings
- Maintain trial-related records
- Prepare regulatory documents
- Submit regulatory documents
- Ensure compliance with study protocols
- Ensure regulatory compliance
- Collaborate with cross-functional teams
- Support trial operations
- Resolve trial issues
- Monitor trial progress
- Track trial progress
- Manage site communications
- Ensure timely delivery of study materials
- Build relationships with site staff
- Maintain relationships with stakeholders
- Facilitate smooth trial operations
- Support project success
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- clinical trial management systems
- relevant software
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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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