ICON plc
Clinical Research Coordinator II (Site Management Associate II)(m/w/x)
Full-timeWith HomeofficeExperienced
Mannheim, Frankfurt am Main
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ICICON Clinical Research Germany GmbH
Site Management Associate - sponsor dedicated(m/w/x)
Mannheim, Frankfurt am Main
Full-timeRemoteExperienced
Nejo AI Summary
Monitoring clinical trial sites and ensuring GCP compliance for a global CRO. Relevant clinical research experience required. 4 weeks vacation, health insurance.
Requirements
- Relevant clinical research experience
- Bachelor's degree in life sciences, healthcare administration, or clinical research
- Clinical research, site management, or monitoring experience
- Solid understanding of clinical trial processes and GCP guidelines
- Strong organizational and project management skills
- Ability to handle multiple priorities and deadlines
- Excellent analytical skills and attention to detail
- Focus on maintaining high-quality standards
- Exceptional communication and interpersonal skills
- Ability to build and maintain relationships with site personnel and teams
- Willingness to travel as required (approx. 25%)
- Interest in the role
Tasks
- Support management and monitoring of clinical trial sites
- Ensure compliance with study protocols and GCP guidelines
- Coordinate monitoring activities at clinical trial sites
- Resolve site-related issues promptly
- Prepare and review regulatory documents
- Ensure site activities comply with GCP and regulations
- Collaborate with cross-functional teams
- Facilitate effective communication and support for trial sites
- Track site performance metrics
- Analyze data to enhance site management efficiency
- Provide reports on site performance
- Participate in training initiatives
- Mentor junior staff in clinical trial management
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Flexible country-specific optional benefits
- 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 Clinical Research Germany GmbH 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 Clinical Research Germany GmbH
Site Management Associate - sponsor dedicated(m/w/x)
Mannheim, Frankfurt am Main
Full-timeRemoteExperienced
Nejo AI Summary
Monitoring clinical trial sites and ensuring GCP compliance for a global CRO. Relevant clinical research experience required. 4 weeks vacation, health insurance.
Requirements
- Relevant clinical research experience
- Bachelor's degree in life sciences, healthcare administration, or clinical research
- Clinical research, site management, or monitoring experience
- Solid understanding of clinical trial processes and GCP guidelines
- Strong organizational and project management skills
- Ability to handle multiple priorities and deadlines
- Excellent analytical skills and attention to detail
- Focus on maintaining high-quality standards
- Exceptional communication and interpersonal skills
- Ability to build and maintain relationships with site personnel and teams
- Willingness to travel as required (approx. 25%)
- Interest in the role
Tasks
- Support management and monitoring of clinical trial sites
- Ensure compliance with study protocols and GCP guidelines
- Coordinate monitoring activities at clinical trial sites
- Resolve site-related issues promptly
- Prepare and review regulatory documents
- Ensure site activities comply with GCP and regulations
- Collaborate with cross-functional teams
- Facilitate effective communication and support for trial sites
- Track site performance metrics
- Analyze data to enhance site management efficiency
- Provide reports on site performance
- Participate in training initiatives
- Mentor junior staff in clinical trial management
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Flexible country-specific optional benefits
- 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 Clinical Research Germany GmbH 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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
ICON Clinical Research Germany GmbH
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
Not a perfect match?
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