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Senior Clinical Research Associate(m/w/x)
Description
In this role, you will oversee clinical trial activities, ensuring compliance with protocols and regulations. Daily tasks will involve monitoring sites, conducting visits, and collaborating with teams to maintain data integrity and participant safety.
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Requirements
- •Advanced degree in life sciences, nursing, or medicine
- •Extensive experience as a Clinical Research Associate
- •Strong understanding of clinical trial processes and regulatory requirements
- •Proven ability to manage multiple sites and projects
- •Strong organizational and problem-solving skills
- •Expertise in monitoring practices and data integrity
- •Proficiency in relevant clinical trial software and tools
- •Excellent communication and interpersonal skills
- •Stakeholder management skills
- •Ability to influence and drive compliance
- •Ability to travel at least 60% of the time
- •Possession of a valid driver’s license
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
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-timeWith HomeofficeSeniorMannheim
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Senior Clinical Research Associate(m/w/x)
The AI Job Search Engine
Description
In this role, you will oversee clinical trial activities, ensuring compliance with protocols and regulations. Daily tasks will involve monitoring sites, conducting visits, and collaborating with teams to maintain data integrity and participant safety.
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
- •Strong understanding of clinical trial processes and regulatory requirements
- •Proven ability to manage multiple sites and projects
- •Strong organizational and problem-solving skills
- •Expertise in monitoring practices and data integrity
- •Proficiency in relevant clinical trial software and tools
- •Excellent communication and interpersonal skills
- •Stakeholder management skills
- •Ability to influence and drive compliance
- •Ability to travel at least 60% of the time
- •Possession of a valid driver’s license
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
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.
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