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Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Monitoring clinical trial sites for biotech studies, ensuring protocol adherence and data integrity. Extensive clinical research monitoring experience and advanced life sciences degree required. Work on global biotech clinical trials.
Requirements
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Proven ability to manage multiple sites and projects
- Expertise in monitoring practices and data integrity
- Excellent communication skills in German and English
Tasks
- Monitor clinical trial sites for protocol adherence
- Conduct site visits to assess performance and resolve issues
- Collaborate with teams for accurate data collection and reporting
- Provide training and guidance to site staff and CRAs
- Build and maintain relationships with site personnel and stakeholders
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- clinical trial software
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
- Flexible optional benefits
Not a perfect match?
- ICON plcFull-timeWith HomeofficeSeniorFrankfurt am Main
- 176 ICON Clinical Research Germany GmbH
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Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Monitoring clinical trial sites for biotech studies, ensuring protocol adherence and data integrity. Extensive clinical research monitoring experience and advanced life sciences degree required. Work on global biotech clinical trials.
Requirements
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Proven ability to manage multiple sites and projects
- Expertise in monitoring practices and data integrity
- Excellent communication skills in German and English
Tasks
- Monitor clinical trial sites for protocol adherence
- Conduct site visits to assess performance and resolve issues
- Collaborate with teams for accurate data collection and reporting
- Provide training and guidance to site staff and CRAs
- Build and maintain relationships with site personnel and stakeholders
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- clinical trial software
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
- Flexible optional benefits
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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