176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSenior
Mannheim
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ICICON plc
Clinical Research Associate II / Senior CRA(m/w/x)
Mannheim
Full-timeWith Home OfficeSenior
Nejo AI Summary
Monitoring clinical trial sites for protocol and regulatory adherence, conducting site visits for a global CRO. Advanced life sciences degree and extensive clinical research monitoring experience required. Global travel, 24-hour professional support.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive Clinical Research Associate experience
- Strong understanding of clinical trial processes
- Strong understanding of regulatory requirements
- Proven ability to manage multiple sites and projects
- Strong organizational skills
- Strong problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in clinical trial software and tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence and drive compliance
- Ability to travel at least 60% (international/domestic)
- Valid driver’s license
Tasks
- Monitor clinical trial sites for protocol, regulatory, and GCP adherence
- Conduct site visits
- Assess site performance
- Resolve site issues
- Provide site support
- Collaborate with cross-functional teams for timely and accurate data collection and reporting
- Provide training and guidance to site staff and CRAs
- Build and maintain effective relationships with site personnel and stakeholders
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- 24-hour professional support
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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ICICON plc
Clinical Research Associate II / Senior CRA(m/w/x)
Mannheim
Full-timeWith Home OfficeSenior
Nejo AI Summary
Monitoring clinical trial sites for protocol and regulatory adherence, conducting site visits for a global CRO. Advanced life sciences degree and extensive clinical research monitoring experience required. Global travel, 24-hour professional support.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive Clinical Research Associate experience
- Strong understanding of clinical trial processes
- Strong understanding of regulatory requirements
- Proven ability to manage multiple sites and projects
- Strong organizational skills
- Strong problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in clinical trial software and tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence and drive compliance
- Ability to travel at least 60% (international/domestic)
- Valid driver’s license
Tasks
- Monitor clinical trial sites for protocol, regulatory, and GCP adherence
- Conduct site visits
- Assess site performance
- Resolve site issues
- Provide site support
- Collaborate with cross-functional teams for timely and accurate data collection and reporting
- Provide training and guidance to site staff and CRAs
- Build and maintain effective relationships with site personnel and stakeholders
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- 24-hour professional support
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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