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CRA II Clinical Research Associate(m/w/x)
Designing and analyzing clinical trials, interpreting complex medical data for innovative treatments. Minimum 2 years CRA experience required. Global Employee Assistance Programme, life assurance.
Requirements
- Relevant clinical trial monitoring experience
- Bachelor's degree in scientific or healthcare field
- Minimum 2 years as Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational and communication skills
- Attention to detail
- Ability to work independently
- Ability to work collaboratively
- Ability to work in fast-paced environment
- Willingness to travel as required (approx. 60%)
Tasks
- Design and analyze clinical trials
- Interpret complex medical data
- Contribute to innovative treatments
- Conduct site qualification visits
- Initiate clinical trial sites
- Monitor clinical trial sites
- Conduct site close-out visits
- Ensure protocol compliance
- Maintain data integrity
- Ensure patient safety
- Collaborate with investigators
- Work with site staff
- Perform data review
- Resolve data queries
- Prepare study documentation
- Review study documentation
- Contribute to clinical study reports
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
- 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
Not a perfect match?
- ICON plcFull-timeWith HomeofficeExperiencedFrankfurt am Main
- ICON plc
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CRA II Clinical Research Associate(m/w/x)
Designing and analyzing clinical trials, interpreting complex medical data for innovative treatments. Minimum 2 years CRA experience required. Global Employee Assistance Programme, life assurance.
Requirements
- Relevant clinical trial monitoring experience
- Bachelor's degree in scientific or healthcare field
- Minimum 2 years as Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational and communication skills
- Attention to detail
- Ability to work independently
- Ability to work collaboratively
- Ability to work in fast-paced environment
- Willingness to travel as required (approx. 60%)
Tasks
- Design and analyze clinical trials
- Interpret complex medical data
- Contribute to innovative treatments
- Conduct site qualification visits
- Initiate clinical trial sites
- Monitor clinical trial sites
- Conduct site close-out visits
- Ensure protocol compliance
- Maintain data integrity
- Ensure patient safety
- Collaborate with investigators
- Work with site staff
- Perform data review
- Resolve data queries
- Prepare study documentation
- Review study documentation
- Contribute to clinical study reports
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
- 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
About the Company
ICON Clinical Research Germany GmbH
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
Not a perfect match?
- ICON plc
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Early Development Clinical Research Associate II(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor Dedicated(m/w/x)
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