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AOAO Foundation

Senior Project Manager Clinical Operations(m/w/x)

Zizers
Vollzeit, Teilzeitmit HomeofficeSenior

Planning and managing clinical studies for a global surgical education non-profit. 2-3 years managing clinical trials in pharma, biotech, CRO, or healthcare required. Flexible working hours and location, supplementary vacation days.

Anforderungen

  • MSc, PhD in scientific or healthcare field or equivalent training/experience
  • 2-3 years managing clinical trials/studies in pharmaceutical, biotech, CRO, or healthcare setting, including prior monitoring experience
  • Knowledge of clinical research operations, including interpretation/implementation of regulations/ICH/GCP, ISO guidelines
  • Core understanding of medical terminology and methodological aspects of clinical trial activities
  • Experience in interactions with outside and inside customers
  • Ability to work on complex/multiple projects and exercise critical thinking with minimal supervision
  • Solid attention to detail and excellent organization skills
  • Solid interpersonal and communication skills (written and oral)
  • Ability to establish priorities, operate with urgency, and collaborate with study team, cross-functional members, and external partners/vendors
  • Problem-solving skills, leadership skills, self-motivation, and adaptability to dynamic environment
  • Flexibility and customer-focused mindset
  • Proficiency in English; other languages are a plus

Aufgaben

  • Plan and manage clinical studies
  • Manage project portfolio for assigned clients
  • Support clinical operations team
  • Develop and track budgets
  • Train team on budget development
  • Conduct site initiation, monitoring, and close-out visits
  • Develop Clinical Investigation Plans and Case Report Forms
  • Create essential documents for clinical studies
  • Validate and control clinical data quality
  • Compile and archive study documents
  • Review study budgets periodically
  • Provide study data status to management and clients
  • Maintain contact with Principal Investigators and Study Nurses
  • Evaluate clinical data with Biostatistician, Medical Advisor, and Medical Writer
  • Generate and present study budgets
  • Define and inform resource allocation
  • Negotiate contracts with study sites
  • Serve as main client contact
  • Represent AO ITC in Research Commissions
  • Plan and coordinate annual research budget
  • Manage and oversee dedicated research activities
  • Align tasks with ISO 9001 quality management standards
  • Contribute to quality system maintenance and improvement
  • Undertake additional responsibilities as assigned

Berufserfahrung

  • 2 - 3 Jahre

Ausbildung

  • Doktor / Ph.D.

Sprachen

  • Englischfließend

Benefits

Flexibles Arbeiten

  • Flexible working hours and location

Modernes Büro

  • Modern infrastructure

Mehr Urlaubstage

  • Supplementary vacation days

Betriebliche Altersvorsorge

  • Pension scheme contributions

Weiterbildungsangebote

  • Internal skills training
  • Support for continued education
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens AO Foundation 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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