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Denn f\u00fcr uns steht fest: Forschung bildet das Fundament unserer aller Zukunft. Wir bei AstraZeneca stellen die Wissenschaft in den Mittelpunkt unseres Handelns. Sie spornt uns an, die Grenzen des M\u00f6glichen stetig zu erweitern und Neues zu schaffen. Wir glauben an die Kraft von Ideen und treiben sie vorw\u00e4rts, um die Behandlung von Krankheiten grundlegend zu verbessern. Mit Leidenschaft arbeiten wir jeden Tag daran, das Leben von Menschen durch Wissenschaft zu verbessern. In unserem Bereich Site Management & Monitoring findet mit der Durchf\u00fchrung der klinischen Studien ein entscheidender Schritt zur Entwicklung unserer innovativen Medikamente statt, um diese m\u00f6glichst schnell und umfangreich erprobt als moderne Therapieoptionen f\u00fcr Patient:innen verf\u00fcgbar zu machen. Unsere Studienteams arbeiten dabei in einem anspruchsvollen und komplexen Umfeld, in dem es auf exzellente Teamarbeit und kompetente Spezialisten gleicherma\u00dfen ankommt. Als Field Clinical Advisor (FCA) (m/w/) - Cell Therapy sind Sie Teil des globalen Cell Therapy Clinical Operations Teams. Sie spielen eine entscheidende Rolle bei der erfolgreichen Durchf\u00fchrung von klinischen Studien in der Zelltherapie, indem sie Rekrutierung, Bindung und Sicherheitsmanagement vorantreiben. Dar\u00fcber hinaus erm\u00f6glichen sie eine fr\u00fchzeitige Generierung von Insights. FCAs konzentrieren sich auf Protokollexpertise und -schulungen, die Optimierung der Patient:innenreisen sowie die Einbindung in die Zelltherapie-Pipeline. Die Funktion arbeitet eng mit anderen CTCO-Funktionen, Clinical Development und Medical Affairs \u00fcber mehrere Indikationen und Abteilungen hinweg zusammen, um das vielf\u00e4ltige Zelltherapie-Portfolio von AstraZeneca zu f\u00f6rdern. Wenn Sie jetzt denken \u201eHier ist meine Zukunft!\u201c, dann freuen wir uns auf Ihre Bewerbung als Field Clinical Advisor (m/w/d) Cell Therapy. Finden auch Sie einen Arbeitsplatz mit hervorragenden Perspektiven, bei dem Sie Ihr Potenzial voll aussch\u00f6pfen k\u00f6nnen. Einfluss nehmen: Aufbau von Wissen \u00fcber die Zelltherapie-Pipeline von AstraZeneca \u00fcber mehrere Indikationen und Assets hinweg. Vermittlung der Zelltherapie-Strategie von AstraZeneca, des Portfolio-Umfangs und der Produktdifferenzierung; Sicherstellung einer regelkonformen Kommunikation \u00fcber alle Regionen hinweg. Systematische Bewertung von Bildungsbedarfen \u00fcber alle Sites hinweg, Bereitstellung von fortgeschrittenen Protokollschulungen und Eskalation von Mustern an das globale Clinical Development Team mit Empfehlungen f\u00fcr unternehmensweite L\u00f6sungen. Erfassung relevanter Erkenntnisse aus dem Feld (Machbarkeit, operative Engp\u00e4sse, Patient:innenpfade) und Weiterleitung an globale und lokale Partner, um eine fr\u00fchzeitige Risikoidentifizierung zu erm\u00f6glichen und Protokoll-/Prozessanpassungen zu durchzuf\u00fchren. Implementierung zielgerichteter Protokollschulungen (z. B. Anwendung von Ein-/Ausschlusskriterien), um Rekrutierungsraten zu erh\u00f6hen, Screen-Fehler zu reduzieren und Abbr\u00fcche zu minimieren. Funktion als prim\u00e4rer Ansprechpartner im Feld f\u00fcr Protokoll- und klinische Fragestellungen - Bewertung und Eskalation, Leitung von Ursachenanalysen sowie Implementierung von Korrektur-/Pr\u00e4ventionsma\u00dfnahmen zur Reduzierung von Abweichungen und Datenabfragen. Systematisches Erfassen von Site-spezifischen Erkenntnissen, Zusammenfassung von Trends f\u00fcr Studienteams und Partner sowie Einflussnahme auf Protokoll-/Prozessanpassungen und deren Skalierung. Koordination der Lieferung \u00fcber CTCO-Abteilungen, Clinical Development, Medical Affairs, Supply/Logistik, Patient Operations und Country Operations, um eine schnelle, zuverl\u00e4ssige Unterst\u00fctzung f\u00fcr Partner und Studienzentren sicherzustellen. Aufrechterhaltung aktueller Kenntnisse der lokalen Vorschriften, Leitlinien, Verhaltenskodizes sowie AstraZeneca-Richtlinien; \u00dcbersetzung der Anforderungen in praktische Ma\u00dfnahmen auf Site-Ebene und Unterst\u00fctzung der Inspektionsbereitschaft. Direkte Verbesserung der Geschwindigkeit, Qualit\u00e4t und Konsistenz von AstraZeneca\u2018 s Zelltherapie-Studien - Verk\u00fcrzung von Durchlaufzeiten, Erh\u00f6hung der Protokolltreue und Beschleunigung des Patient:innenzugangs zu innovativen Behandlungen. St\u00e4rken beweisen: Studienabschluss in einem verwandten Fachgebiet, vorzugsweise in Biowissenschaften, oder gleichwertige Qualifikation; weiterf\u00fchrender Abschluss (z.B. PhD) w\u00fcnschenswert Mehrj\u00e4hrige Erfahrung in der klinischen Forschung oder in medizinischen Au\u00dfendienstrollen mit Fokus in der Onkologie/H\u00e4matologie/Immunologie/Seltenen Erkrankungen oder fortgeschrittenen Therapien Direkte CAR\u2011T/Zelltherapie-Erfahrung Fundierte technische Kenntnisse und umfassende Erfahrung im Bereich klinischer Operationen, insbesondere hinsichtlich der Patient:innenreisen in der Zelltherapie Sehr gute Kenntnisse des klinischen Studienprozesses, der Verfahrensdokumente und der internationalen GMP-ICH-GCP-Richtlinien Ausgezeichnetes Partnermanagement mit der F\u00e4higkeit, komplexe Protokolle in praktische Ma\u00dfnahmen auf Site-Ebene zu \u00fcbersetzen Ausgepr\u00e4gte Patient:innen- und Site-Zentrierung sowie gute Kenntnisse der relevanten lokalen und internationalen Vorschriften NachgewieseneF\u00e4higkeit, Priorit\u00e4ten, Ressourcen, Leistungsziele und Projektinitiativen in einem regionalen und lokalen Umfeld zu setzen und zu steuern Hohe Datenorientierung sowie nachweisbare Erfahrung in datenbezogenen Ans\u00e4tzen zur Identifikation von Trends, Risiken und Chancen f\u00fcr operative Verbesserungen F\u00e4higkeit, effizientere und effektivere Methoden/Prozesse der klinischen Entwicklung zu identifizieren und zu f\u00f6rdern, mit Fokus auf Kern KPIs wie Zuverl\u00e4ssigkeit, Produktivit\u00e4t, Kosten und Qualit\u00e4t Hervorragende schriftliche und m\u00fcndliche Kommunikations-f\u00e4higkeiten, Verhandlungsgeschick, Kollaborationsf\u00e4higkeit und zwischenmenschliche Kompetenz, mit der F\u00e4higkeit, auf allen Ebenen der Organisation effektiv zusammenzuarbeiten Bereitschaft, mindestens 50-80 % regional / national zu reisen, um Studienzentren und Programmanforderungen zu unterst\u00fctzen. Sehr gute Deutsch- sowie Englischkenntnisse, sowie gute Lernf\u00e4higkeit und Anpassungsf\u00e4higkeit im Umgang mit IT-Systemen. Freuen Sie sich auf: eine attraktive Pipeline und innovative Produkte individuelle Entwicklungsm\u00f6glichkeiten und den Fokus auf lebenslanges Lernen viel Vertrauen, Wertsch\u00e4tzung und Raum f\u00fcr Mitgestaltung in einem fokussierten und leidenschaftlichen Team ein diverses, inklusives und vorurteilsfreies Arbeitsumfeld, das der Charta der Vielfalt verpflichtet ist, Unterschiede nicht nur zul\u00e4sst, sondern aktiv f\u00f6rdert und Bewerbungen aller qualifizierten Bewerbenden, unabh\u00e4ngig von ihren Merkmalen begr\u00fc\u00dft und ber\u00fccksichtigt ein nachhaltiges Unternehmen, welches bis 2030 entlang der gesamten Wertsch\u00f6pfungskette CO2-negativ wird ein attraktives Benefitpaket wie z.B. EGYM Wellpass, Corporate Benefits und vieles mehr Wollen Sie Teil unserer Mission werden und die Lebensqualit\u00e4t zahlreicher Patient:innen steigern? Dann bewerben Sie sich jetzt. 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