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Clinical Research Lead Assistant(m/w/x)
Administrative support for clinical trials documentation and regulatory submissions at global healthcare intelligence organization. Extensive clinical trial support experience and CTMS proficiency required. Involvement in international clinical research projects.
Requirements
- Advanced degree or certification in relevant field
- Extensive clinical trial support experience
- Understanding of clinical trial processes
- Strong organizational and multitasking skills
- Proficiency in clinical trial management systems
- Attention to detail in documentation
- Excellent communication and interpersonal skills
- Strong problem-solving skills
Tasks
- Provide administrative support for clinical trials
- Manage documentation and trial-related records
- Coordinate and schedule project meetings
- Prepare and submit regulatory documents
- Ensure compliance with protocols and requirements
- Collaborate with cross-functional teams
- Resolve operational issues during studies
- Monitor and track trial progress
- Manage communications with clinical sites
- Ensure timely delivery of study materials
- Build relationships with site staff and stakeholders
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- Clinical trial management systems
Benefits
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
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-timeRemoteExperiencedFrankfurt am Main
- ICON plc
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Clinical Research Lead Assistant(m/w/x)
Administrative support for clinical trials documentation and regulatory submissions at global healthcare intelligence organization. Extensive clinical trial support experience and CTMS proficiency required. Involvement in international clinical research projects.
Requirements
- Advanced degree or certification in relevant field
- Extensive clinical trial support experience
- Understanding of clinical trial processes
- Strong organizational and multitasking skills
- Proficiency in clinical trial management systems
- Attention to detail in documentation
- Excellent communication and interpersonal skills
- Strong problem-solving skills
Tasks
- Provide administrative support for clinical trials
- Manage documentation and trial-related records
- Coordinate and schedule project meetings
- Prepare and submit regulatory documents
- Ensure compliance with protocols and requirements
- Collaborate with cross-functional teams
- Resolve operational issues during studies
- Monitor and track trial progress
- Manage communications with clinical sites
- Ensure timely delivery of study materials
- Build relationships with site staff and stakeholders
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- Clinical trial management systems
Benefits
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
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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Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Senior Clinical Research Associate(m/w/x)
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Clinical Site Manager(m/w/x)
Full-timeRemoteSeniorFrankfurt am Main - ICON plc
Senior CRA (Sponsor dedicated)(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
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