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Junior Clinical Research Associate - sponsor dedicated(m/w/x)
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials in a sponsor-dedicated setting. Minimum 1 year clinical research experience required. Global Employee Assistance Programme, life assurance.
Requirements
- Relevant clinical trial monitoring experience
- Bachelor's degree in scientific or healthcare field
- Minimum 1 year clinical research experience (e.g., Study Coordinator)
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational and communication skills, attention to detail
- Ability to work independently and collaboratively
- Ability to work in a fast-paced environment
- Willingness to travel as required (approx. 60%)
- Interest in the role
Tasks
- Conduct site qualification visits
- Initiate clinical trial sites
- Monitor clinical trial sites
- Close out clinical trial sites
- Ensure protocol compliance
- Maintain data integrity
- Safeguard patient safety
- Collaborate with investigators
- Work with site staff
- Review clinical data
- Resolve data queries
- Prepare study documentation
- Review study protocols
- Contribute to clinical study reports
Work Experience
- 1 year
Education
- Bachelor's degree
Languages
- German – Business Fluent
- 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
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Junior Clinical Research Associate - sponsor dedicated(m/w/x)
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials in a sponsor-dedicated setting. Minimum 1 year clinical research experience required. Global Employee Assistance Programme, life assurance.
Requirements
- Relevant clinical trial monitoring experience
- Bachelor's degree in scientific or healthcare field
- Minimum 1 year clinical research experience (e.g., Study Coordinator)
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational and communication skills, attention to detail
- Ability to work independently and collaboratively
- Ability to work in a fast-paced environment
- Willingness to travel as required (approx. 60%)
- Interest in the role
Tasks
- Conduct site qualification visits
- Initiate clinical trial sites
- Monitor clinical trial sites
- Close out clinical trial sites
- Ensure protocol compliance
- Maintain data integrity
- Safeguard patient safety
- Collaborate with investigators
- Work with site staff
- Review clinical data
- Resolve data queries
- Prepare study documentation
- Review study protocols
- Contribute to clinical study reports
Work Experience
- 1 year
Education
- Bachelor's degree
Languages
- German – Business Fluent
- 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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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