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Clinical Research Associate II - FSP(m/w/x)
Monitoring clinical trial sites for pharmaceutical clients under a functional service provider model. In-depth knowledge of ICH-GCP guidelines and clinical trial regulations required. Extensive travel to clinical sites, working independently on client projects.
Requirements
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills
- Ability to work independently and collaboratively in a fast-paced environment
- Ability to travel at least 60% of the time and possess a valid driver’s license
Tasks
- Conduct site qualification visits for clinical trials
- Initiate clinical trial site visits
- Monitor clinical trial sites
- Perform close-out visits for clinical trials
- Ensure protocol compliance throughout the trial process
- Maintain data integrity and patient safety
- Collaborate with investigators and site staff
- Facilitate smooth study conduct
- Review data and resolve queries for high-quality clinical data
- Prepare and review study documentation
- Draft clinical study reports and protocols
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
- Flexible optional benefits
Not a perfect match?
- ICON plcFull-timeWith HomeofficeExperiencedFrankfurt am Main
- ICON plc
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Clinical Research Associate II - FSP(m/w/x)
Monitoring clinical trial sites for pharmaceutical clients under a functional service provider model. In-depth knowledge of ICH-GCP guidelines and clinical trial regulations required. Extensive travel to clinical sites, working independently on client projects.
Requirements
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills
- Ability to work independently and collaboratively in a fast-paced environment
- Ability to travel at least 60% of the time and possess a valid driver’s license
Tasks
- Conduct site qualification visits for clinical trials
- Initiate clinical trial site visits
- Monitor clinical trial sites
- Perform close-out visits for clinical trials
- Ensure protocol compliance throughout the trial process
- Maintain data integrity and patient safety
- Collaborate with investigators and site staff
- Facilitate smooth study conduct
- Review data and resolve queries for high-quality clinical data
- Prepare and review study documentation
- Draft clinical study reports and protocols
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
- Flexible optional benefits
About the Company
176 ICON Clinical Research Germany GmbH
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on innovative treatments.
Not a perfect match?
- ICON plc
Clinical Research Associate II(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate - French / German Speaking - FSP(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
CRA II/ Senior CRA(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main