Senior Pharmacovigilance Officer, Team Lead – Medical Device Experience

Vaga não está no LinkedIn

🕒 Julho 23

🇵🇱 Polônia – Remoto

⏰ Tempo Integral

🟠 Sênior

👔 Gerente

🗣️🇺🇸🇬🇧 Inglês obrigatório

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Logo of ERGOMED

ERGOMED

1001 - 5000 funcionários

Fundada em 1997

💼 Consultoria

🏥 Saúde

📦 Logística

Consulting • Healthcare • Logistics

ERGOMED é um grupo global que oferece serviços especializados para as indústrias de biotecnologia e farmacêutica. Opera sob diferentes linhas de serviço, incluindo Ergomed Clinical Research, PrimeVigilance, e ADAMAS Consulting, e é dedicada a fornecer capacidades completas de organização de pesquisa clínica (CRO). Com foco em oncologia, doenças raras e estudos complexos, também oferece serviços completos de farmacovigilância e informações médicas, bem como auditorias abrangentes de GxP. A Ergomed está comprometida em apoiar o desenvolvimento de medicamentos com presença global em cerca de 100 países.

Descrição

• Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader and Line Manages ICSR staff • Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process • Assures and exerts activities leading to effective cooperation with clients in the area of ICSR Management • Contributes to achieving company´s goals and objectives • Works under supervision of ICSR Operational Lead • Provides support to other activities undertaken by the project team on behalf of the client and the company • Creates and maintains project specific KPIs for contracted ICSR activities • Proposes process changes to ICSR Operational Lead • Manages ICSR deviations with ICSR Operational Lead support • Reviews trackers and timesheet data and ensures accuracy • Is involved in ICSR processing and 2nd QC of cases • Supports other departments, as approved and instructed by ICSR Operational Lead • Operates as the assigned team SME

🎯 Requisitos

• Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance • Strong previous work experience in pharmacovigilance with minimum 1 year of work experience in line manager role • Medical Device experience required • Excellent communication (written and verbal) skills • Organization skills, including attention to details and multitasking • Delegation skills • Planning and time management • Technical skills • Team working • English – fluent (spoken, written) • Advanced literacy (MS Office)

🏖️ Benefícios

• The chance to keep growing while you help protect patients • A passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting • An environment built on kindness, flexibility, growth, and belonging

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