Senior Trial Vendor Manager – UK, Ireland, France

🕒 Maio 14

🇬🇧 Reino Unido – Remoto (RU)

⏰ Tempo Integral

🟠 Sênior

👔 Gerente

🇬🇧 Patrocina Visto de Trabalhador Qualificado UK

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Parexel

SiteLinkedInTodas as Vagas

10.000+ funcionários

Fundada em 1983

⚕️ Seguro de Saúde

🧬 Biotecnologia

💊 Farmacêutico

💰 Venture Round em 1990-01

Healthcare Insurance • Biotechnology • Pharmaceuticals

Parexel é uma das maiores organizações de pesquisa clínica (CROs) do mundo, oferecendo serviços abrangentes para o processo de desenvolvimento clínico das Fases I a IV. A empresa é especializada em gestão de portfólio, gestão de ensaios clínicos, estratégia regulatória, acesso ao mercado e gestão do ciclo de vida para biofarmacêuticos. A Parexel busca acelerar a chegada de medicamentos que transformam vidas ao mercado, alavancando sua expertise clínica, regulatória e terapêutica. Com uma equipe global de mais de 21. 000 profissionais, a Parexel trabalha para integrar insights de pacientes e desenhos de estudo inovadores a fim de desenvolver tratamentos em áreas terapêuticas como oncologia, neurociência, doenças raras, entre outras. Seu foco está na condução de ensaios clínicos eficientes e centrados no paciente.

Descrição

• Independently manage all vendor-related aspects of global clinical trials to deliver study outcomes within schedule, budget, quality/compliance and performance standards. • Proactively manage vendor-related risks and potential issues. • Collaborate closely with study team lead and study team members during study lifetime. • Review vendor related protocol sections during protocol development. • Manage interface with vendors in cooperation with vendor partner functions. • Support contract negotiations, if required. • Accountable for vendor cost control, budget review, invoice reconciliation and PO close-out. • Ensure vendors meet quality and service level standards in their service delivery for the trial. • Attend vendor kick-off meeting for VSM supported categories. • Monitor site activation progress and address related issues and risk.

🎯 Requisitos

• Bachelor's degree or equivalent degree is required, with advanced degree preferred. • 3+ years working experience and excellent knowledge of the clinical operation processes and vendor management. • Excellent knowledge of GxP and ICH regulations. • Very good knowledge of clinical trial design and mapping to supplier requirements. • Experience in User Acceptance testing for e-COA and IRT. • Very strong vendor management skills; outsourcing, contracting, and sourcing of clinical services. • Results-driven: demonstrated ability of completing projects on time. • Strong influencing and negotiation skills. • Strong relationship building and good written and oral communication skills. • Strong problem solving, negotiation, deadline driven and conflict resolution skills. • Excellent interpersonal skills (team player). • Strong organizational awareness; advanced planning and project management skills. • Proven networking skills and ability to share knowledge and experience amongst colleagues. • Proficient in written and spoken English.

🏖️ Benefícios

• Professional development opportunities • Open and friendly work environment