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Clinical Research Associate (CRA)(m/w/x)
Overseeing clinical trial sites from initial qualification to final close-out for a global CRO. In-depth knowledge of clinical trial processes and ICH-GCP guidelines required. Frequent site visits across diverse locations.
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
- Fluency in English and German language
- Ability to work independently and collaboratively
- Ability to travel at least 60% of the time
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 and data integrity
- Prioritize patient safety throughout the trial process
- Collaborate with investigators and site staff
- Review and resolve data 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
- Competitive retirement planning
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 (CRA)(m/w/x)
Overseeing clinical trial sites from initial qualification to final close-out for a global CRO. In-depth knowledge of clinical trial processes and ICH-GCP guidelines required. Frequent site visits across diverse locations.
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
- Fluency in English and German language
- Ability to work independently and collaboratively
- Ability to travel at least 60% of the time
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 and data integrity
- Prioritize patient safety throughout the trial process
- Collaborate with investigators and site staff
- Review and resolve data 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
- Competitive retirement planning
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
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Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
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