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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
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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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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.
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