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CRA II/ Senior CRA(m/w/x)
Overseeing clinical trial sites from qualification to close-out for new drug development at a global CRO. 2+ years of clinical research monitoring experience and in-depth ICH-GCP knowledge required. Frequent site visits for diverse 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 in a fast-paced environment
- Excellent communication skills in German and English
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 and resolve data queries
- Prepare and review study documentation
- Draft clinical study reports
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Healthcare & Fitness
- Health insurance offerings
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
- Flexible optional benefits
Not a perfect match?
- ICON plcFull-timeRemoteExperiencedFrankfurt am Main
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CRA II/ Senior CRA(m/w/x)
Overseeing clinical trial sites from qualification to close-out for new drug development at a global CRO. 2+ years of clinical research monitoring experience and in-depth ICH-GCP knowledge required. Frequent site visits for diverse 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 in a fast-paced environment
- Excellent communication skills in German and English
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 and resolve data queries
- Prepare and review study documentation
- Draft clinical study reports
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Healthcare & Fitness
- Health insurance offerings
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
- Flexible optional benefits
About the Company
176 ICON Clinical Research Germany GmbH
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on innovative treatments.
Not a perfect match?
- ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main