ICON plc
(Senior) Clinical Research Associate (CRA) - sponsor dedicated(m/w/x)
Full-timeRemoteNot specified
Frankfurt am Main
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ICON plc(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Description
You will ensure the integrity of clinical trials by monitoring site performance and fostering strong relationships with stakeholders to guarantee participant safety and regulatory compliance.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Advanced degree in life sciences, nursing, or medicine
- •Extensive experience as Clinical Research Associate
- •Understanding of clinical trial processes and regulations
- •Management of multiple sites and projects
- •Strong organizational and problem-solving skills
- •Expertise in monitoring and data integrity
- •Proficiency in clinical trial software
- •Excellent communication and stakeholder management skills
- •Ability to influence and drive compliance
- •Fluency in German and English
- •Willingness to travel at least 60%
- •Possession of a valid driver’s license
Education
Master's degree
Work Experience
approx. 4 - 6 years
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 teams for accurate data collection
- •Train site staff on trial conduct standards
- •Provide guidance to other research associates
- •Maintain relationships with site personnel and stakeholders
Tools & Technologies
clinical trial software
Languages
German – Business Fluent
English – Business Fluent
Benefits
More Vacation Days
- •Various annual leave entitlements
Healthcare & Fitness
- •Range of health insurance offerings
- •Health assessments
Retirement Plans
- •Competitive retirement planning offerings
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
- •Reasonable accommodations
Childcare
- •Childcare vouchers
Company Bike
- •Bike purchase schemes
Corporate Discounts
- •Discounted gym memberships
Public Transport Subsidies
- •Subsidised travel passes
Informal Culture
- •Inclusive and accessible environment
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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IC
ICON plc(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
New Job?Nejo!
The AI Job Search Engine
Description
You will ensure the integrity of clinical trials by monitoring site performance and fostering strong relationships with stakeholders to guarantee participant safety and regulatory compliance.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Advanced degree in life sciences, nursing, or medicine
- •Extensive experience as Clinical Research Associate
- •Understanding of clinical trial processes and regulations
- •Management of multiple sites and projects
- •Strong organizational and problem-solving skills
- •Expertise in monitoring and data integrity
- •Proficiency in clinical trial software
- •Excellent communication and stakeholder management skills
- •Ability to influence and drive compliance
- •Fluency in German and English
- •Willingness to travel at least 60%
- •Possession of a valid driver’s license
Education
Master's degree
Work Experience
approx. 4 - 6 years
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 teams for accurate data collection
- •Train site staff on trial conduct standards
- •Provide guidance to other research associates
- •Maintain relationships with site personnel and stakeholders
Tools & Technologies
clinical trial software
Languages
German – Business Fluent
English – Business Fluent
Benefits
More Vacation Days
- •Various annual leave entitlements
Healthcare & Fitness
- •Range of health insurance offerings
- •Health assessments
Retirement Plans
- •Competitive retirement planning offerings
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
- •Reasonable accommodations
Childcare
- •Childcare vouchers
Company Bike
- •Bike purchase schemes
Corporate Discounts
- •Discounted gym memberships
Public Transport Subsidies
- •Subsidised travel passes
Informal Culture
- •Inclusive and accessible environment
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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