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Clinical Research Associate - Sponsor dedicated(m/w/x)
Clinical trial management for a specific pharmaceutical sponsor, from site qualification to close-out, at a global healthcare intelligence CRO. 2+ years CRA experience and English/German fluency required. Regular site visits across multiple locations expected.
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 with attention to detail
- Fluency in English and German language
- Ability to work independently and collaboratively in a fast-paced environment
- Ability to travel at least 60% of the time and possess a valid driver’s license
Tasks
- Conduct site qualification visits for clinical trials
- Initiate clinical trial sites
- Monitor clinical trial progress
- Perform close-out visits for clinical trials
- Ensure protocol compliance throughout the trial process
- Maintain data integrity and patient safety
- Collaborate with investigators and site staff
- Facilitate smooth study conduct
- Review data and resolve queries
- Prepare and review study documentation
- Draft clinical study reports and protocols
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – 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 2 / CRA 2(m/w/x)
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Clinical Research Associate - Sponsor dedicated(m/w/x)
Clinical trial management for a specific pharmaceutical sponsor, from site qualification to close-out, at a global healthcare intelligence CRO. 2+ years CRA experience and English/German fluency required. Regular site visits across multiple locations expected.
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 with attention to detail
- Fluency in English and German language
- Ability to work independently and collaboratively in a fast-paced environment
- Ability to travel at least 60% of the time and possess a valid driver’s license
Tasks
- Conduct site qualification visits for clinical trials
- Initiate clinical trial sites
- Monitor clinical trial progress
- Perform close-out visits for clinical trials
- Ensure protocol compliance throughout the trial process
- Maintain data integrity and patient safety
- Collaborate with investigators and site staff
- Facilitate smooth study conduct
- Review data and resolve queries
- Prepare and review study documentation
- Draft clinical study reports and protocols
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – 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
CRA II/ Senior CRA(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) Clinical Research Associate - sponsor dedicated(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA RDS GmbH
Clinical Research Associate 2 / CRA 2(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main