ICON plc
Senior CRA (Sponsor Dedicated)(m/w/x)
Full-timeWith HomeofficeSenior
Frankfurt am Main
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ICICON plc
Senior CRA (Sponsor dedicated)(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
On-site monitoring of clinical trial sites for a dedicated sponsor's drug development. Advanced degree in life sciences and extensive clinical trial monitoring experience required. Focus on a single sponsor's clinical trial portfolio.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as Clinical Research Associate
- Understanding of clinical trial processes and regulations
- Ability to manage multiple sites and projects
- Strong organizational and problem-solving skills
- Expertise in monitoring practices and data integrity
- Proficiency in clinical trial software and tools
- Excellent communication and stakeholder management skills
- Ability to influence and drive compliance
- Ability to travel 60% of the time
- Possession of a valid driver’s license
Tasks
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory and GCP standards
- Conduct site visits to assess performance
- Resolve site issues to ensure trial execution
- Collaborate with cross-functional teams for data reporting
- Train and guide site staff and colleagues
- Maintain high standards of clinical trial conduct
- Build effective relationships with site personnel
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- clinical trial software
Benefits
Competitive Pay
- Competitive salary
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
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) Clinical Research Associate - sponsor dedicated(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor Dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Senior CRA(m/w/x)
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Senior Clinical Research Associate (SCRA) - sponsor dedicated(m/w/x)
Full-timeRemoteSeniorFrankfurt am Main
ICICON plc
Senior CRA (Sponsor dedicated)(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
On-site monitoring of clinical trial sites for a dedicated sponsor's drug development. Advanced degree in life sciences and extensive clinical trial monitoring experience required. Focus on a single sponsor's clinical trial portfolio.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as Clinical Research Associate
- Understanding of clinical trial processes and regulations
- Ability to manage multiple sites and projects
- Strong organizational and problem-solving skills
- Expertise in monitoring practices and data integrity
- Proficiency in clinical trial software and tools
- Excellent communication and stakeholder management skills
- Ability to influence and drive compliance
- Ability to travel 60% of the time
- Possession of a valid driver’s license
Tasks
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory and GCP standards
- Conduct site visits to assess performance
- Resolve site issues to ensure trial execution
- Collaborate with cross-functional teams for data reporting
- Train and guide site staff and colleagues
- Maintain high standards of clinical trial conduct
- Build effective relationships with site personnel
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- clinical trial software
Benefits
Competitive Pay
- Competitive salary
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
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
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Senior CRA(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