ICON plc
Sr. Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeExperienced
Wien
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ICICON plc
Clinical Research Associate - Sponsor Dedicated(m/w/x)
Wien
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Monitoring clinical trials for a global CRO, focusing on ICH-GCP compliance and medical data evaluation. Relevant clinical trial monitoring experience required. Annual leave entitlements, health insurance, and retirement planning.
Requirements
- Relevant clinical trial monitoring experience
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines
- Expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Good social skills for timely query resolution
- Willingness to travel as required (approximately 60%)
- Encouraged to apply even if unsure about meeting all requirements
Tasks
- Coordinate study setup and monitoring activities
- Complete accurate study status reports
- Maintain study documentation
- Run sponsor-generated queries efficiently
- Participate in study documentation preparation and review
- Conduct feasibility studies for new proposals
- Develop strong relationships with stakeholders
- Collaborate with clinical investigators and site staff
- Ensure patient safety and compliance with procedures
- Maintain regulatory requirements
Work Experience
- approx. 1 - 4 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
- Competitive 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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Not a perfect match?
- ICON plc
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Full-timeWith HomeofficeSeniorWien - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Full-timeWith HomeofficeExperiencedWienfrom 4,000 / month - IQVIA
Clinical Research Associate I or II(m/w/x)
Full-timeWith HomeofficeJuniorWienfrom 3,600 / month - IQVIA
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Full-timeWith HomeofficeSeniorWienfrom 4,200 / month
ICICON plc
Clinical Research Associate - Sponsor Dedicated(m/w/x)
Wien
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Monitoring clinical trials for a global CRO, focusing on ICH-GCP compliance and medical data evaluation. Relevant clinical trial monitoring experience required. Annual leave entitlements, health insurance, and retirement planning.
Requirements
- Relevant clinical trial monitoring experience
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines
- Expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Good social skills for timely query resolution
- Willingness to travel as required (approximately 60%)
- Encouraged to apply even if unsure about meeting all requirements
Tasks
- Coordinate study setup and monitoring activities
- Complete accurate study status reports
- Maintain study documentation
- Run sponsor-generated queries efficiently
- Participate in study documentation preparation and review
- Conduct feasibility studies for new proposals
- Develop strong relationships with stakeholders
- Collaborate with clinical investigators and site staff
- Ensure patient safety and compliance with procedures
- Maintain regulatory requirements
Work Experience
- approx. 1 - 4 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
- Competitive 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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Not a perfect match?
- ICON plc
Sr. Clinical Research Associate(m/w/x)
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Full-timeWith HomeofficeSeniorWien - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Full-timeWith HomeofficeExperiencedWienfrom 4,000 / month - IQVIA
Clinical Research Associate I or II(m/w/x)
Full-timeWith HomeofficeJuniorWienfrom 3,600 / month - IQVIA
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Full-timeWith HomeofficeSeniorWienfrom 4,200 / month