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Clinical Research Associate - French / German Speaking - FSP(m/w/x)
Description
In this role, you will be integral to the success of clinical trials, ensuring compliance and data integrity while collaborating with site staff. Daily tasks will involve site visits, data review, and contributing to essential study documentation.
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Requirements
- •Bachelor's degree in a scientific or healthcare-related field
- •Minimum of 2 years of experience as a Clinical Research Associate
- •In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- •Strong organizational and communication skills
- •Ability to work independently and collaboratively
- •Ability to travel at least 60% of the time
Education
Work Experience
2 years
Tasks
- •Conduct site qualification visits
- •Initiate clinical trial sites
- •Monitor clinical trial progress
- •Perform close-out visits for trials
- •Ensure protocol compliance
- •Maintain data integrity
- •Prioritize patient safety during trials
- •Collaborate with investigators and site staff
- •Facilitate smooth study conduct
- •Review data and resolve queries
- •Prepare and review study documentation
- •Draft clinical study reports
Languages
French – Business Fluent
German – Business Fluent
Benefits
More Vacation Days
- •Various annual leave entitlements
Healthcare & Fitness
- •Health insurance offerings
Retirement Plans
- •Retirement planning offerings
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
Additional Allowances
- •Flexible optional benefits
- ICON plcFull-timeRemoteExperiencedFrankfurt am Main
- ICON plc
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Clinical Research Associate - French / German Speaking - FSP(m/w/x)
The AI Job Search Engine
Description
In this role, you will be integral to the success of clinical trials, ensuring compliance and data integrity while collaborating with site staff. Daily tasks will involve site visits, data review, and contributing to essential study documentation.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Bachelor's degree in a scientific or healthcare-related field
- •Minimum of 2 years of experience as a Clinical Research Associate
- •In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- •Strong organizational and communication skills
- •Ability to work independently and collaboratively
- •Ability to travel at least 60% of the time
Education
Work Experience
2 years
Tasks
- •Conduct site qualification visits
- •Initiate clinical trial sites
- •Monitor clinical trial progress
- •Perform close-out visits for trials
- •Ensure protocol compliance
- •Maintain data integrity
- •Prioritize patient safety during trials
- •Collaborate with investigators and site staff
- •Facilitate smooth study conduct
- •Review data and resolve queries
- •Prepare and review study documentation
- •Draft clinical study reports
Languages
French – Business Fluent
German – Business Fluent
Benefits
More Vacation Days
- •Various annual leave entitlements
Healthcare & Fitness
- •Health insurance offerings
Retirement Plans
- •Retirement planning offerings
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
Additional Allowances
- •Flexible optional benefits
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
- ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
Clinical Research Associate II - FSP(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
CRA II/ Senior CRA(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main