IQVIA
Clinical Research Associate or SrCRA(m/w/x)
Full-timeWith HomeofficeExperienced
Basel
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IQIQVIA
Regulatory and Start Up Specialist(m/w/x)
Basel
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Country-level site activation and ongoing maintenance for clinical trials at global healthcare intelligence firm. Submissions experience in Switzerland or Belgium required. Single point of contact for studies, 30 days vacation.
Requirements
- German language fluency
- Submissions experience in Switzerland or Belgium
- Degree in life sciences, related field, or equivalent
- Three years clinical research or relevant experience
- Knowledge of clinical systems and procedures
- Knowledge of corporate standards
- Ability to apply GCP/ICH and regulatory guidelines
- Knowledge of local regulations and SOPs
- Understanding of regulated clinical trial environment
- Knowledge of drug development process
Tasks
- Perform country-level Site Activation activities
- Follow local and international regulations
- Adhere to SOPs and contractual guidelines
- Execute ongoing site maintenance activities
- Act as Single Point of Contact for studies
- Liaise with sites and project management teams
- Ensure quality of deliverables and timelines
- Distribute completed documents to project members
- Prepare and review site regulatory documents
- Maintain internal systems and tracking tools
- Provide feedback on site performance metrics
- Establish and agree on project timelines
- Implement monitoring measures and contingency plans
- Communicate completion of regulatory and contractual documents
- Track progress of ethics and ICF documents
- Manage Investigator Pack release documents
- Provide local expertise for project planning
- Perform quality control of site documents
- Communicate directly with sponsors on specific initiatives
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
Tools & Technologies
- GCP
- ICH
- SOPs
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA 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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IQIQVIA
Regulatory and Start Up Specialist(m/w/x)
Basel
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Country-level site activation and ongoing maintenance for clinical trials at global healthcare intelligence firm. Submissions experience in Switzerland or Belgium required. Single point of contact for studies, 30 days vacation.
Requirements
- German language fluency
- Submissions experience in Switzerland or Belgium
- Degree in life sciences, related field, or equivalent
- Three years clinical research or relevant experience
- Knowledge of clinical systems and procedures
- Knowledge of corporate standards
- Ability to apply GCP/ICH and regulatory guidelines
- Knowledge of local regulations and SOPs
- Understanding of regulated clinical trial environment
- Knowledge of drug development process
Tasks
- Perform country-level Site Activation activities
- Follow local and international regulations
- Adhere to SOPs and contractual guidelines
- Execute ongoing site maintenance activities
- Act as Single Point of Contact for studies
- Liaise with sites and project management teams
- Ensure quality of deliverables and timelines
- Distribute completed documents to project members
- Prepare and review site regulatory documents
- Maintain internal systems and tracking tools
- Provide feedback on site performance metrics
- Establish and agree on project timelines
- Implement monitoring measures and contingency plans
- Communicate completion of regulatory and contractual documents
- Track progress of ethics and ICF documents
- Manage Investigator Pack release documents
- Provide local expertise for project planning
- Perform quality control of site documents
- Communicate directly with sponsors on specific initiatives
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
Tools & Technologies
- GCP
- ICH
- SOPs
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA 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
IQVIA
Industry
Healthcare
Description
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
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