ICON plc
Sr. Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeExperienced
Wien
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ICICON plc
Senior Clinical Research Associate(m/w/x)
Wien
Full-timeWith Home OfficeSenior
Nejo AI Summary
Oversight of clinical study sites, ensuring protocol and regulatory compliance for a global CRO. Extensive clinical monitoring experience required. Frequent site visits, with global EAP and 24-hour professional support.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive Clinical Research Associate experience
- Strong understanding of clinical trial processes
- Strong understanding of regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously
- Strong organizational skills
- Strong problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence and drive compliance in complex environment
- Ability to travel at least 60% (international and domestic)
- Valid driver’s license
Tasks
- Monitor clinical trial sites for protocol, regulatory, and GCP adherence.
- Conduct site visits.
- Assess site performance.
- Resolve site-related issues.
- Provide support for successful trial execution.
- Collaborate with cross-functional teams for timely, accurate data collection.
- Collaborate with cross-functional teams for timely, accurate data reporting.
- Train and guide site staff and CRAs on trial conduct.
- Build and maintain effective relationships with site personnel and stakeholders.
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- 24-hour professional support
- Life assurance
Additional Allowances
- 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.
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ICICON plc
Senior Clinical Research Associate(m/w/x)
Wien
Full-timeWith Home OfficeSenior
Nejo AI Summary
Oversight of clinical study sites, ensuring protocol and regulatory compliance for a global CRO. Extensive clinical monitoring experience required. Frequent site visits, with global EAP and 24-hour professional support.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive Clinical Research Associate experience
- Strong understanding of clinical trial processes
- Strong understanding of regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously
- Strong organizational skills
- Strong problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence and drive compliance in complex environment
- Ability to travel at least 60% (international and domestic)
- Valid driver’s license
Tasks
- Monitor clinical trial sites for protocol, regulatory, and GCP adherence.
- Conduct site visits.
- Assess site performance.
- Resolve site-related issues.
- Provide support for successful trial execution.
- Collaborate with cross-functional teams for timely, accurate data collection.
- Collaborate with cross-functional teams for timely, accurate data reporting.
- Train and guide site staff and CRAs on trial conduct.
- Build and maintain effective relationships with site personnel and stakeholders.
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- 24-hour professional support
- Life assurance
Additional Allowances
- 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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Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Full-timeWith HomeofficeSeniorWienfrom 4,200 / month - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Full-timeWith HomeofficeExperiencedWienfrom 4,000 / month - AOP Health
Clinical Site Management Lead(m/w/x)
Full-timeWith HomeofficeSeniorWienfrom 45,080 / year - IQVIA
Clinical Research Associate I or II(m/w/x)
Full-timeWith HomeofficeJuniorWienfrom 3,600 / month