[Uza-379] | Senior Clinical Trial Supply Chain Manager With

[Uza-379] | Senior Clinical Trial Supply Chain Manager With
Empresa:

*Nombre Oculto*


Detalles de la oferta

LOCATION: CORK, IRELAND (Funded relocation)EU/UK Passport or Stamp 4 requiredThis role will be accountable for continuous process improvement and shared learning to drive a culture that fosters innovation, efficiency, and productivity.Key ResponsibilitiesLeading the Clinical Trial Supply Management departmentRecruiting and retaining appropriately qualified staff, recommending, and implementing staffing decisions.Managing and supervision of staff including performance management, coaching, mentoring and robust development, reward, and recognition.Delivering on time, within the scope, and on budget as a department.Managing organization as a business.Maintaining credibility with clinical and functional partners with proactive communication.Supporting innovation and process optimization to speed drug development by providing support and guidance for direct reports.Focusing on fostering an environment of integrated teamwork and partnership via shared learning, accountability, and influencing others with and without authority.Accountable for the oversight of staff translating clinical trial protocols into material demand, investigator site inventory strategies, and clinical trial supply implementation activities (i.e., site inventory management, CT label, CT material expiration management, etc.) during clinical trial execution including robust assumptions, modeling, and risk plans.Accountable to build and maintain relationships with key clinical partners.RequirementsBachelor's degree, preferably in health care or sciences related field or 5+ years of work experience in clinical trial research and/or supply chain3+ years of experience preferred in one or more of the following areas: clinical trial supply planning, SIM site management/ monitoring, clinical development/SAP systems.Knowledge of GMPs/GCPs and other regulations related to CT MaterialsMediation and problem-solving skills in both group and individual interactions.Ability to lead under high pressure and expectations.Effective written and verbal communication skills in multi-cultural settings.High initiative, flexible and positive attitude.High degree of autonomyExceptional business acumen and project planning capabilitiesFluent English, Spanish a plusAdditional Information/RequirementsWork outside of core hours may be required to support the portfolio across the globeMinimal travel may be required, both domestic and international.Job Types: Full-time, PermanentSalary: From 50,000.00€ per year
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Fuente: Whatjobs_Ppc

Requisitos

[Uza-379] | Senior Clinical Trial Supply Chain Manager With
Empresa:

*Nombre Oculto*


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