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Clinical Research Associate II(m/w/x)
Conducting site qualification, initiation, and monitoring visits at a global clinical research organization. Minimum 2 years Clinical Research Associate experience required. Regular travel for site monitoring.
Requirements
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years Clinical Research Associate experience
- Knowledge of clinical trial processes and regulations
- Strong organizational, communication, and detail-oriented skills
- Ability to work independently and collaboratively
- Ability to travel 60% and driver’s license
Tasks
- Conduct site qualification and initiation visits
- Perform clinical trial monitoring and close-out visits
- Ensure protocol compliance and patient safety
- Maintain data integrity throughout the trial process
- Collaborate with investigators and site staff
- Review data and resolve queries for quality
- Prepare and review study protocols
- Draft and evaluate clinical study reports
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- ICH-GCP guidelines
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Range of health insurance
- Health assessments
Retirement Plans
- Competitive 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
Not a perfect match?
- 176 ICON Clinical Research Germany GmbHFull-timeRemoteExperiencedFrankfurt am Main
- ICON plc
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Clinical Research Associate II(m/w/x)
Conducting site qualification, initiation, and monitoring visits at a global clinical research organization. Minimum 2 years Clinical Research Associate experience required. Regular travel for site monitoring.
Requirements
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years Clinical Research Associate experience
- Knowledge of clinical trial processes and regulations
- Strong organizational, communication, and detail-oriented skills
- Ability to work independently and collaboratively
- Ability to travel 60% and driver’s license
Tasks
- Conduct site qualification and initiation visits
- Perform clinical trial monitoring and close-out visits
- Ensure protocol compliance and patient safety
- Maintain data integrity throughout the trial process
- Collaborate with investigators and site staff
- Review data and resolve queries for quality
- Prepare and review study protocols
- Draft and evaluate clinical study reports
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- ICH-GCP guidelines
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Range of health insurance
- Health assessments
Retirement Plans
- Competitive 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
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Not a perfect match?
- 176 ICON Clinical Research Germany GmbH
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Clinical Research Associate - Sponsor Dedicated(m/w/x)
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