Clinical Trial Assistant, Sponsor-dedicated
vor 2 Wochen
Wenn Sie auf der Suche nach einer Aufgabe sind, in der Sie Ihr Organisationstalent und Ihr gutes Auge für Details ebenso einsetzen können wie Ihre Kommunikationsfähigkeiten gegenüber so unterschiedlicher Zielgruppen wie Prüfärzten, Studienteams und Zulassungsbehörden, dann ist dies eine hervorragende Gelegenheit. Kommen Sie zu uns und überzeugen Sie sich selbst, warum mehr als 90% der 20 weltweit führenden Pharmaunternehmen seit vielen Jahren zu unseren Kunden zählen
**Was Sie von uns erwarten dürfen**:
- eine bedeutungsvolle Tätigkeit in einem stabilen, diversen, erfolgreichen und angesehenen Unternehmen
- eine attraktive und konkurrenzfähige Vergütung, einschließlich lokaler Sonderzahlungen
- eine echte Work-Life-Balance
- flexible Arbeitszeiten sowie betriebliche Regelungen zum Freizeitausgleich
- ein umfassendes Onboarding mit Unterstützung durch Ihren persönlichen Mentor
- einen unbefristeten Arbeitsvertrag
- einen attraktivern arbeitgeberfinanzierten Pensionsplan
- hervorragende Fortbildungs
- und Entwicklungsmöglichkeiten sowie Unterstützung bei Ihren persönlichen Weiterbildungsplänen
- kontinuierliche Unterstützung durch Ihren Line Manager, Ihr Team und mehr als 20'000 Kolleg*innen weltweit
**Ihre Aufgaben**:
- Unterstützung unserer lokalen Studienteams in allen Aspekten klinischer Studien, von der Auswahl der Studienzentren über die Bereitstellung der notwendigen Materialien und Medikamente bis zum Close-Out
- Koordination aller internen und externen Beteiligten an Ihren Studien für einen reibungslosen Ablauf
- Dokumentenmanagement, inkl. fristgerechte Zusammenstellung von Datenpaketen für die Zulassungsbehörden, Vorbereitung von Besuchen an den Studienzentren sowie die fortlaufende Sicherstellung einer hohen Datenqualität bis hin zur Archivierung
- Rechnungsbearbeitung sowie fortlaufende Prüfung und Pflege der Finanzdatensysteme
**Ihr Background**:
- Hochschulabschluss in einem relevanten Fachgebiet wie z.B. Biologie, Biochemie, Chemie, Gesundheitswesen, Pharmakologie, Medizin usw.; alternativ eine abgeschlossene Berufsausbildung im Bereich Administration / Gesundheit / Pflege oder gleichwertige Berufserfahrung (z. B. als Study Nurse, Research Nurse, Studienkoordinator*in....)
- Berufserfahrung in der Administration klinischer Studien in Österreich
- Kenntnis der geltenden Österreicher und internationalen Regularien bei klinischen Studien wie z.B. ICH / GCP
- praktische Kenntnisse im Bereich Good Documentation Practices (GDP)
- sicherer Umgang mit IT-Anwendungen wie MS Office (einschließlich guter MS Excel-Kenntnisse) und klinischen IT-Anwendungen (Veeva Vault usw.)
- ausgezeichnete Organisations
- und Projektmanagementfähigkeiten mit einem ausgeprägten Sinn für Details und einem hohen Verantwortungsbewusstsein
- ** ausgezeichnete Kommunikationsfähigkeiten in verhandlungssicherem Deutsch sowie gute Englischkenntnisse in Wort und Schrift sind ein Muss**
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
**Did you know?**
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
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