Director - Clinical Operations Europe (m/f/d)
vor 1 Monat
At Elanco (NYSE: ELAN) – it all starts with animals
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today
Position Description:
As the Director of Clinical Operations Europe, you will play a pivotal role in overseeing study support services and leading a dynamic team of 5 individuals. You will be responsible for driving excellence across three key areas: monitoring and clinical research associate support, R&D study material logistics, and data and document management. Additionally, you will spearhead initiatives to identify efficiencies and enhance processes, contributing significantly to the successful execution of our global R&D strategy at a regional level.
Functions, Duties, Tasks:
Leadership and Team Management:
Lead a team of 5 professionals, ensuring performance accountability, resource forecasting, and fostering a culture of excellence and collaborationPartner strategically with internal stakeholders and third-party providers to optimize cross-functional collaboration and drive process improvementsProvide study support services, resolving roadblocks, and fostering customer-centric behaviorCollaborate closely with department peers and global colleaguesClinical Development:
Provide support across all aspects of internal and external GxP studiesInternalize field study programs by establishing a network of Investigators and contributing to clinical strategy developmentAct as the sponsor representative in GCP studies and assist with regulatory submissionsR&D Study Material Logistics and Management:
Ensure compliant logistics for R&D study materials and maintaining relationships with suppliersManage R&D material logistics, including shipments, warehousing, and compliance with dangerous goods regulationsSupport global study material management and adhere to logistics budgetData and Document Management:
Manage R&D archives and archiving processes, including GxP studies, regulatory documents, and sample retentionOversee local electronic data capture processes and collaborate with global Data Management for expansion and standardizationQualifications (education, experience and/or training, required certifications):
DVM and PhD, or Master and PhD in a relevant field or equivalent5+ years of R&D experience, including clinical trial management and/or logisticsProven track record of managing cross-functional teams and driving process improvementsStrong understanding of GxP regulations; logistics knowledge preferredExcellent leadership and communication skills, effective problem-solving and customer-centricityProficient in Microsoft Suite; quick learner of new toolsFluent in German and EnglishLegal authorization for employment in GermanyWHAT WE OFFER
Pension plan with employer matching contribution30 days vacationHealth and fitness benefitsSubsidized Job Ticket and bike leasingEncourage individual initiative and provide opportunities for personal developmentWork as part of a dynamic team in an international company-
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