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Clinical Research Associate - French / German Speaking - FSP(m/w/x)
Conducting site qualification and monitoring visits for pharmaceutical clinical trials at a global CRO. 2+ years CRA experience, ICH-GCP knowledge, and French/German fluency essential. Exposure to diverse international clinical studies.
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
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
Work Experience
- 2 years
Education
- Bachelor's degree
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
Not a perfect match?
- ICON plcFull-timeRemoteExperiencedFrankfurt am Main
- 176 ICON Clinical Research Germany GmbH
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Clinical Research Associate - French / German Speaking - FSP(m/w/x)
Conducting site qualification and monitoring visits for pharmaceutical clinical trials at a global CRO. 2+ years CRA experience, ICH-GCP knowledge, and French/German fluency essential. Exposure to diverse international clinical studies.
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
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
Work Experience
- 2 years
Education
- Bachelor's degree
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.
Not a perfect match?
- ICON plc
Clinical Research Associate (CRA)(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 - ICON plc
Clinical Research Associate - Sponsor dedicated(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