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Senior Clinical Research Associate(m/w/x)
Description
As a Senior Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance and data integrity while supporting site staff and fostering collaboration across teams for successful trial execution.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Advanced degree in 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 and interpersonal skills
- •Ability to travel at least 60% of the time
- •Fluency in German and English
Education
Work Experience
approx. 4 - 6 years
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
Languages
German – Business Fluent
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
- 176 ICON Clinical Research Germany GmbHFull-timeRemoteSeniorFrankfurt am Main
- ICON plc
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Senior Clinical Research Associate(m/w/x)
The AI Job Search Engine
Description
As a Senior Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance and data integrity while supporting site staff and fostering collaboration across teams for successful trial execution.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Advanced degree in 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 and interpersonal skills
- •Ability to travel at least 60% of the time
- •Fluency in German and English
Education
Work Experience
approx. 4 - 6 years
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
Languages
German – Business Fluent
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
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
- 176 ICON Clinical Research Germany GmbH
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