ICON plc
Senior CRA (Sponsor dedicated)(m/w/x)
Full-timeWith HomeofficeSenior
Frankfurt am Main
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ICICON plc
Clinical Research Associate(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
Monitoring clinical trial sites for protocol adherence and GCP compliance. Extensive CRA experience and regulatory knowledge required. 6 weeks vacation, company car for private use.
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
- Proven ability to manage multiple projects
- Strong organizational skills
- Strong problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in relevant clinical trial software
- Proficiency in relevant clinical trial tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence within a complex environment
- Ability to drive compliance within a complex environment
- Ability to travel at least 40-60% of the time
- Encouraged to apply even if not meeting all requirements
Tasks
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory requirements
- Uphold Good Clinical Practice (GCP) standards
- Conduct site visits to assess performance
- Resolve site issues and provide support
- Ensure successful trial execution
- Collaborate with cross-functional teams
- Ensure timely data collection
- Ensure accurate data collection
- Ensure timely data reporting
- Ensure accurate data reporting
- Train site staff on trial conduct
- Guide site staff on trial conduct
- Train other CRAs on trial conduct
- Guide other CRAs on trial conduct
- Build relationships with site personnel
- Maintain relationships with site personnel
- Build relationships with stakeholders
- Maintain relationships with stakeholders
- Facilitate smooth trial operations
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- clinical trial software
- clinical trial tools
Benefits
Healthcare & Fitness
- Health insurance
- Health assessments
Retirement Plans
- Retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- 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(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
Monitoring clinical trial sites for protocol adherence and GCP compliance. Extensive CRA experience and regulatory knowledge required. 6 weeks vacation, company car for private use.
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
- Proven ability to manage multiple projects
- Strong organizational skills
- Strong problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in relevant clinical trial software
- Proficiency in relevant clinical trial tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence within a complex environment
- Ability to drive compliance within a complex environment
- Ability to travel at least 40-60% of the time
- Encouraged to apply even if not meeting all requirements
Tasks
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory requirements
- Uphold Good Clinical Practice (GCP) standards
- Conduct site visits to assess performance
- Resolve site issues and provide support
- Ensure successful trial execution
- Collaborate with cross-functional teams
- Ensure timely data collection
- Ensure accurate data collection
- Ensure timely data reporting
- Ensure accurate data reporting
- Train site staff on trial conduct
- Guide site staff on trial conduct
- Train other CRAs on trial conduct
- Guide other CRAs on trial conduct
- Build relationships with site personnel
- Maintain relationships with site personnel
- Build relationships with stakeholders
- Maintain relationships with stakeholders
- Facilitate smooth trial operations
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- clinical trial software
- clinical trial tools
Benefits
Healthcare & Fitness
- Health insurance
- Health assessments
Retirement Plans
- Retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- 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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