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Clinical Research Associate (CRA) - sponsor dedicated(m/w/x)
Sponsor-dedicated clinical trial monitoring and site initiation for a global CRO. Minimum 2 years CRA experience with ICH-GCP knowledge required. 4 weeks vacation, health insurance, retirement planning.
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 and 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
- 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 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
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Clinical Research Associate (CRA) - sponsor dedicated(m/w/x)
Sponsor-dedicated clinical trial monitoring and site initiation for a global CRO. Minimum 2 years CRA experience with ICH-GCP knowledge required. 4 weeks vacation, health insurance, retirement planning.
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 and 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
- 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 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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
850 RPS Research Services Austria
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
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