QEH IQVIA RDS Eastern Holdings GmbH
Site Activation & Administrative Coordinator(m/w/x)
Full-timeOn-siteNot specified
Wien
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
PSPSI CRO
Clinical Site Coordinator(m/w/x)
Wien
VollzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
Liaising between Sponsor/CROs and clinical study sites for stronger study delivery, managing monitoring visits and patient enrollment at a Site Enabling Services organization. University degree in Life Science (pharmacy, nursing, lab analytics) preferred. Flexible working hours.
Anforderungen
- University degree in Life Science, preferably pharmacy, nursing or lab analytics
- Minimum 2 years on-the-job experience as site coordinator
- Ability to work in fast-paced environment with short timelines
- Effective communication in stressful situations and problem-solving ability
- Flexibility in working hours
- Fluent English and Local Language
Aufgaben
- Liaise between the Sponsor/CRO and the site.
- Ensure timely responses to feasibility questions.
- Assist with scheduling and preparing for monitoring visits.
- Respond to monitors during monitoring visits.
- Track patient enrollment.
- Support teams in meeting project timelines.
- Support teams in achieving enrollment goals.
- Maintain study-specific and general document tracking.
- Perform timely and accurate data entry into EDC systems.
- Resolve data clarification queries promptly.
- Report adverse events and protocol deviations promptly.
- Follow up on adverse events and protocol deviations promptly.
- Manage investigational products and clinical supplies properly.
- Collect, handle, and maintain site-specific regulatory documents.
- Facilitate and support site contract and budget negotiations.
- Support Investigator and site payment processes.
- Schedule and perform study procedures as required.
- Prepare for study audits and regulatory inspections.
- Participate in study audits and regulatory inspections.
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Flexible working hours
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens PSI CRO 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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PSPSI CRO
Clinical Site Coordinator(m/w/x)
Wien
VollzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
Liaising between Sponsor/CROs and clinical study sites for stronger study delivery, managing monitoring visits and patient enrollment at a Site Enabling Services organization. University degree in Life Science (pharmacy, nursing, lab analytics) preferred. Flexible working hours.
Anforderungen
- University degree in Life Science, preferably pharmacy, nursing or lab analytics
- Minimum 2 years on-the-job experience as site coordinator
- Ability to work in fast-paced environment with short timelines
- Effective communication in stressful situations and problem-solving ability
- Flexibility in working hours
- Fluent English and Local Language
Aufgaben
- Liaise between the Sponsor/CRO and the site.
- Ensure timely responses to feasibility questions.
- Assist with scheduling and preparing for monitoring visits.
- Respond to monitors during monitoring visits.
- Track patient enrollment.
- Support teams in meeting project timelines.
- Support teams in achieving enrollment goals.
- Maintain study-specific and general document tracking.
- Perform timely and accurate data entry into EDC systems.
- Resolve data clarification queries promptly.
- Report adverse events and protocol deviations promptly.
- Follow up on adverse events and protocol deviations promptly.
- Manage investigational products and clinical supplies properly.
- Collect, handle, and maintain site-specific regulatory documents.
- Facilitate and support site contract and budget negotiations.
- Support Investigator and site payment processes.
- Schedule and perform study procedures as required.
- Prepare for study audits and regulatory inspections.
- Participate in study audits and regulatory inspections.
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Flexible working hours
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens PSI CRO 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.
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
PSI CRO
Branche
Healthcare
Beschreibung
The company is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation.
Not a perfect match?
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