ICON plc
Clinical Research Associate II / Senior CRA(m/w/x)
Full-timeWith HomeofficeSenior
Mannheim
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ICICON plc
Clinical Research Coordinator II (Site Management Associate II)(m/w/x)
Mannheim, Frankfurt am Main
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Coordinating monitoring activities and resolving site issues for clinical trials. Bachelor's degree and clinical research experience required. 4 weeks vacation, health insurance.
Requirements
- Bachelor’s degree in life sciences, healthcare administration, or clinical research
- Experience in clinical research, site management, or monitoring
- 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 effective relationships with site personnel and cross-functional teams
- Fluent German
- Ability to go to office in Munich
- Interest in the role
- Encouraged to apply even if not meeting all requirements
Tasks
- Coordinate monitoring activities at clinical trial sites
- Ensure adherence to study protocols
- Resolve site-related issues promptly
- Assist in preparing regulatory documents
- Review regulatory documents
- Ensure site activities comply with GCP
- Ensure site activities comply with applicable regulations
- Collaborate with cross-functional teams
- Facilitate effective communication with trial sites
- Provide support to trial sites
- Track site performance metrics
- Analyze site performance data
- Provide reports on site management efficiency
- Participate in training initiatives
- Mentor junior staff
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – 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
- 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 Coordinator II (Site Management Associate II)(m/w/x)
Mannheim, Frankfurt am Main
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Coordinating monitoring activities and resolving site issues for clinical trials. Bachelor's degree and clinical research experience required. 4 weeks vacation, health insurance.
Requirements
- Bachelor’s degree in life sciences, healthcare administration, or clinical research
- Experience in clinical research, site management, or monitoring
- 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 effective relationships with site personnel and cross-functional teams
- Fluent German
- Ability to go to office in Munich
- Interest in the role
- Encouraged to apply even if not meeting all requirements
Tasks
- Coordinate monitoring activities at clinical trial sites
- Ensure adherence to study protocols
- Resolve site-related issues promptly
- Assist in preparing regulatory documents
- Review regulatory documents
- Ensure site activities comply with GCP
- Ensure site activities comply with applicable regulations
- Collaborate with cross-functional teams
- Facilitate effective communication with trial sites
- Provide support to trial sites
- Track site performance metrics
- Analyze site performance data
- Provide reports on site management efficiency
- Participate in training initiatives
- Mentor junior staff
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – 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
- 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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