ICON plc
Senior Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSenior
Frankfurt am Main
New Job?Nejo!
The AI Job Search Engine
Monitoring clinical trial sites for protocol adherence and GCP standards in Oncology at global clinical research organization. Advanced degree in life sciences or medicine, with Oncology experience, essential. Frequent site visits, global project scope.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as Clinical Research Associate
- Understanding of clinical trial processes and regulations
- Experience in Oncology
- Ability to manage multiple sites and projects
- Strong organizational and problem-solving skills
- Expertise in monitoring practices and site management
- Proficiency in clinical trial software and tools
- Excellent communication and stakeholder management skills
- Ability to influence and drive compliance
- Fluency in German and English
- Ability to travel at least 60%
Tasks
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory and GCP standards
- Conduct site visits to assess performance
- Resolve site issues and provide execution support
- Collaborate with teams for accurate data reporting
- Train and guide site staff and CRAs
- Maintain high standards of clinical trial conduct
- Build effective relationships with site personnel
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- clinical trial software
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
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.
Not a perfect match?
- 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)
Full-timeWith HomeofficeSeniorFrankfurt am Main - ICON plc
(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate (SCRA) - sponsor dedicated(m/w/x)
Full-timeRemoteSeniorFrankfurt am Main
Monitoring clinical trial sites for protocol adherence and GCP standards in Oncology at global clinical research organization. Advanced degree in life sciences or medicine, with Oncology experience, essential. Frequent site visits, global project scope.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as Clinical Research Associate
- Understanding of clinical trial processes and regulations
- Experience in Oncology
- Ability to manage multiple sites and projects
- Strong organizational and problem-solving skills
- Expertise in monitoring practices and site management
- Proficiency in clinical trial software and tools
- Excellent communication and stakeholder management skills
- Ability to influence and drive compliance
- Fluency in German and English
- Ability to travel at least 60%
Tasks
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory and GCP standards
- Conduct site visits to assess performance
- Resolve site issues and provide execution support
- Collaborate with teams for accurate data reporting
- Train and guide site staff and CRAs
- Maintain high standards of clinical trial conduct
- Build effective relationships with site personnel
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- clinical trial software
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
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.
Not a perfect match?
- ICON plc
Senior Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt 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)
Full-timeWith HomeofficeSeniorFrankfurt am Main - ICON plc
(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate (SCRA) - sponsor dedicated(m/w/x)
Full-timeRemoteSeniorFrankfurt am Main