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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 with protocols and regulations while supporting site staff and fostering strong relationships to facilitate 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 a relevant field
- •Extensive experience as a Clinical Research Associate
- •Strong organizational and problem-solving skills
- •Expertise in monitoring practices and data integrity
- •Excellent communication and interpersonal skills
- •Ability to travel at least 60% of the time
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
Tools & Technologies
Languages
English – 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
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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 with protocols and regulations while supporting site staff and fostering strong relationships to facilitate 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 a relevant field
- •Extensive experience as a Clinical Research Associate
- •Strong organizational and problem-solving skills
- •Expertise in monitoring practices and data integrity
- •Excellent communication and interpersonal skills
- •Ability to travel at least 60% of the time
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
Tools & Technologies
Languages
English – 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.
- IQVIA
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