ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Full-timeWith HomeofficeSenior
Frankfurt am Main
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ICICON plc
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
Monitoring clinical trial sites, ensuring protocol adherence and regulatory compliance for a global healthcare intelligence organization. Minimum 2 years Clinical Research Associate experience, with ICH-GCP knowledge, required. Extensive site travel, global trial exposure.
Requirements
- Master or Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years experience as Clinical Research Associate
- Knowledge of clinical trial processes, regulations, and ICH-GCP
- Strong organizational, communication, and detail-oriented skills
- Ability to work independently and collaboratively
- Ability to manage multiple sites and projects
- Expertise in monitoring practices and data integrity
- Excellent communication skills in German and English
- Excellent interpersonal and stakeholder management skills
- Willingness to travel 60% and valid driver’s license
Tasks
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory and GCP standards
- Conduct site visits to assess performance
- Resolve site issues to ensure trial execution
- Collaborate with teams for accurate data reporting
- Train site staff and junior CRAs
- Maintain relationships with site personnel and stakeholders
- Ensure data integrity and participant safety
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- ICH-GCP guidelines
- clinical trial software
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Range of health insurance
- Health assessments
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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Full-timeWith HomeofficeSeniorFrankfurt am Main - ICON plc
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ICICON plc
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
Monitoring clinical trial sites, ensuring protocol adherence and regulatory compliance for a global healthcare intelligence organization. Minimum 2 years Clinical Research Associate experience, with ICH-GCP knowledge, required. Extensive site travel, global trial exposure.
Requirements
- Master or Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years experience as Clinical Research Associate
- Knowledge of clinical trial processes, regulations, and ICH-GCP
- Strong organizational, communication, and detail-oriented skills
- Ability to work independently and collaboratively
- Ability to manage multiple sites and projects
- Expertise in monitoring practices and data integrity
- Excellent communication skills in German and English
- Excellent interpersonal and stakeholder management skills
- Willingness to travel 60% and valid driver’s license
Tasks
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory and GCP standards
- Conduct site visits to assess performance
- Resolve site issues to ensure trial execution
- Collaborate with teams for accurate data reporting
- Train site staff and junior CRAs
- Maintain relationships with site personnel and stakeholders
- Ensure data integrity and participant safety
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- ICH-GCP guidelines
- clinical trial software
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Range of health insurance
- Health assessments
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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 II / Senior Clinical Research Associate Biotech(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
CRA II/ Senior CRA(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 - ICON plc
(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main