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.Reg & Start Up Spec 1(m/w/x)
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
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.Reg & Start Up Spec 1(m/w/x)
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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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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