Takeda
Associate Director, Drug Product Manufacturing Science & Technology(m/w/x)
Vollzeit
Senior
Keine Angabe
Zürich, Opfikon
TA
Takeda Pharmaceuticals International AG1 Monat
Associate Director, Site Start Up and Maintenance(m/w/x)
Management
Vollzeit
Keine Angabe
Zürich
Nejo KI-Zusammenfassung
In this role, you will lead the global clinical operations team, ensuring high-quality site maintenance services through strategic planning and collaboration. Your day-to-day responsibilities will include mentoring staff, analyzing data for effective resource forecasting, and driving innovative solutions to enhance site processes.
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Anforderungen
- •BS degree or international equivalent in life science
- •Extensive experience (≥ 8 years) in Clinical Operations, Project Management, study start-up, site budgeting and contracting, or trial optimization
- •More than 5 years of direct responsibility in site management and oversight of clinical research studies
- •Expertise in clinical trial regulations and ethics committee submissions
- •Expertise in site contract and budget amendments administration
- •Expertise with leading edge trial optimization vendors, tools, and methods
- •Experience in line management and working in a matrix environment
- •Proficiency with software models and database structures
- •Expertise in principles driving site maintenance strategies including site contract amendments
- •Direct experience in the pharmaceutical industry or related field
- •Ability to demonstrate, interpret, explain, represent, and drive unbiased data insights into clinical trials operational delivery
- •Ability to develop deep insights, uncover unmet needs, drive innovation, inspire, develop, collaborate and lead within a global matrixed team
- •Ability to explain data and facilitate decision making processes to be data driven
Bachelor-Abschluss
ODER
Master-Abschluss
Berufserfahrung
8 Jahre
Deine Aufgaben
- •Oversee strategic planning for global site regulatory activities
- •Manage budgeting and contracting maintenance tasks
- •Collaborate with internal and external stakeholders
- •Provide guidance and mentorship to assigned staff
- •Analyze clinical trial intelligence data for resource forecasting
- •Support priority projects through study closure
- •Champion innovative processes and methodologies for site services
- •Partner with CROs and Clinical Operations teams to improve metrics
- •Train Site Start Up and Maintenance Teams on efficient planning
- •Ensure consistent standards across project portfolios
- •Drive implementation of solutions to enhance site maintenance
- •Leverage industry tools for timeline and performance data
- •Monitor adherence to deliverables at country and site levels
- •Lead cross-functional site maintenance teams
- •Serve as a point of escalation for issue resolution
- •Model Takeda’s values in all interactions
Sprachen
Englisch – verhandlungssicher
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Takeda Pharmaceuticals International AG 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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