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Clinical Research Associate II - FSP(m/w/x)
Description
As a Clinical Research Associate II, you will be integral to the success of clinical trials, ensuring compliance and data integrity while collaborating with site staff and investigators. This role involves a mix of site visits, data review, and documentation preparation.
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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
- •Ability to travel at least 60% of the time and possess a valid driver’s license
Education
Work Experience
2 years
Tasks
- •Conduct site qualification visits for clinical trials
- •Initiate clinical trial site visits
- •Monitor clinical trial sites
- •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 for high-quality clinical data
- •Prepare and review study documentation
- •Draft clinical study reports and protocols
Languages
English – 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
- •Flexible optional benefits
- ICON plcFull-timeRemoteExperiencedFrankfurt am Main
- ICON plc
Clinical Research Associate - French / German Speaking - FSP(m/w/x)
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Clinical Research Associate - Sponsor dedicated(m/w/x)
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Clinical Research Associate II - FSP(m/w/x)
The AI Job Search Engine
Description
As a Clinical Research Associate II, you will be integral to the success of clinical trials, ensuring compliance and data integrity while collaborating with site staff and investigators. This role involves a mix of site visits, data review, and documentation preparation.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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
- •Ability to travel at least 60% of the time and possess a valid driver’s license
Education
Work Experience
2 years
Tasks
- •Conduct site qualification visits for clinical trials
- •Initiate clinical trial site visits
- •Monitor clinical trial sites
- •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 for high-quality clinical data
- •Prepare and review study documentation
- •Draft clinical study reports and protocols
Languages
English – 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
- •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.
- ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate - French / German Speaking - FSP(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor dedicated(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 - IQVIA RDS GmbH
Clinical Research Associate 2 / CRA 2(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main