PSI CRO
Clinical Site Coordinator(m/w/x)
Full-timeOn-siteExperienced
Wien
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QAQAT IQVIA RDS Austria GmbH
.Reg & Start Up Spec 1(m/w/x)
Wien
Full-timeOn-siteJunior
Nejo AI Summary
Site activation for clinical trials, serving as single point of contact. 1 year clinical research experience required. Adherence to SOPs and budget guidelines.
Requirements
- 1 year clinical research experience
- Equivalent education, training, and experience
Tasks
- Perform site activation tasks
- Adhere to local and international regulations
- Follow standard operating procedures
- Meet project requirements and budgetary guidelines
- Serve as Single Point of Contact for studies
- Coordinate with investigative sites, Site Activation Manager, and Project Management team
- Ensure quality of deliverables and project timelines
- Perform start up and site activation activities
- Distribute completed documents to sites and project team
- Prepare and review site regulatory documents
- Maintain internal systems and databases with project information
- Review and provide feedback on site performance metrics
- Establish and agree on project planning and timelines
- Implement monitoring measures and contingency plans
- Inform team of completed regulatory and contractual documents
- Track and follow up on document progress and approvals
- Review and control quality of site-provided documents
- Provide local expertise during project planning
- Maintain direct contact with sponsors on specific initiatives
Work Experience
- 1 year
Education
- High school diploma
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of QAT IQVIA RDS Austria GmbH 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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QAQAT IQVIA RDS Austria GmbH
.Reg & Start Up Spec 1(m/w/x)
Wien
Full-timeOn-siteJunior
Nejo AI Summary
Site activation for clinical trials, serving as single point of contact. 1 year clinical research experience required. Adherence to SOPs and budget guidelines.
Requirements
- 1 year clinical research experience
- Equivalent education, training, and experience
Tasks
- Perform site activation tasks
- Adhere to local and international regulations
- Follow standard operating procedures
- Meet project requirements and budgetary guidelines
- Serve as Single Point of Contact for studies
- Coordinate with investigative sites, Site Activation Manager, and Project Management team
- Ensure quality of deliverables and project timelines
- Perform start up and site activation activities
- Distribute completed documents to sites and project team
- Prepare and review site regulatory documents
- Maintain internal systems and databases with project information
- Review and provide feedback on site performance metrics
- Establish and agree on project planning and timelines
- Implement monitoring measures and contingency plans
- Inform team of completed regulatory and contractual documents
- Track and follow up on document progress and approvals
- Review and control quality of site-provided documents
- Provide local expertise during project planning
- Maintain direct contact with sponsors on specific initiatives
Work Experience
- 1 year
Education
- High school diploma
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of QAT IQVIA RDS Austria GmbH 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
QAT IQVIA RDS Austria GmbH
Industry
Healthcare
Description
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
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