IQVIA
Clinical Research Associate or SrCRA(m/w/x)
Vollzeitmit HomeofficeBerufserfahren
Basel
Neuer Job?Nejo!
Die KI-Suchmaschine für Jobs
IQIQVIA
Regulatory and Start Up Specialist(m/w/x)
Basel
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
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.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
Tools & Technologien
- GCP
- ICH
- SOPs
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens IQVIA erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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IQIQVIA
Regulatory and Start Up Specialist(m/w/x)
Basel
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
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.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
Tools & Technologien
- GCP
- ICH
- SOPs
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens IQVIA erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
IQVIA
Branche
Healthcare
Beschreibung
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Noch nicht perfekt?
- IQVIA
Clinical Research Associate or SrCRA(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBasel - ICON plc
Senior Clinical Research Associate(m/w/x)
VollzeitRemoteSeniorBasel - Thermo Fisher Scientific
Site Contract Specialist(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenReinach - IQVIA
Internship as Clinical Research Associate(m/w/x)
VollzeitPraktikummit HomeofficeBasel - Novartis Pharma AG
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Vollzeitmit HomeofficeSeniorBasel