Pharmacovigilance Specialist
Há 2 horas
This is a full-time, regular, 100% home-based role Job Overview Apply knowledge and expertise including complex decision making activities to review, assess and process Safety data and information across service lines.Recognized as specialist in one or more areas.Provide oversight on small to medium service operational projects and act as mentor to junior members of staff.Essential Functions Process safety data in compliance with regulations, SOPs, and project requirements.Perform pharmacovigilance activities: Collect and track Adverse Events (AEs) and endpoint information.Determine event status, enter data into databases, code AEs/products, and write narratives.Conduct literature searches, quality reviews, reconciliation, and case closure.Assess safety data for reportability and ensure timely reporting to regulatory authorities and stakeholders.Maintain project documentation, templates, and workflows.Monitor project metrics, timelines, and deliverables; provide regular updates to management.Ensure compliance with quality standards and project processes.Collaborate with cross-functional teams (clinical, data management, project management) and healthcare professionals.Participate in client communications regarding day-to-day project activities.Train and mentor junior team members; support team development.Contribute to process improvements and efficiency initiatives.Complete all required training and maintain compliance with SOPs.Attend project meetings and provide feedback on operational performance.Perform other duties as assigned.Qualifications Bachelor's Degree in life sciences (mandatory) English Advanced (mandatory) Up to 5 years of relevant pharmacovigilance experience, inclusive of up to 3 years of specific experience in data entry inside Argus and narrative writing inside case processing activities (mandatory) In depth knowledge and understanding of applicable ARGUS Safety Database and any other internal/Client applications.In depth knowledge and understanding of applicable global, regional, local clinical research regulatory requirements.Excellent organizational skills, time management skills, attention to detail and accuracy.Excellent working knowledge of Microsoft Office and web-based applications.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.Learn more at
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Pharmacovigilance Reporting Specialist
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São Paulo, Brasil ICON Tempo inteiroPharmacovigilance Reporting Specialist - Brazil, Sao Paulo (Office Based - Hybrid) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development....
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Pharmacovigilance Reporting Specialist
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Affiliate Pharmacovigilance Manager
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São Paulo, Brasil Eli Lilly and Company Tempo inteiroAffiliate Pharmacovigilance Manager Join to apply for the Affiliate Pharmacovigilance Manager role at Eli Lilly and Company. Purpose The purpose of the Affiliate Pharmacovigilance Manager role is managing the pharmacovigilance processes and procedures of Lilly Affiliate in Brazil, in accordance with the national pharmacovigilance regulations and with the...
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Affiliate Pharmacovigilance Manager
Há 6 dias
São Paulo, Brasil Eli Lilly and Company Tempo inteiroAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...
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Affiliate Pharmacovigilance Manager
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São Paulo, Brasil Eli Lilly and Company Tempo inteiroAffiliate Pharmacovigilance Manager page is loaded## Affiliate Pharmacovigilance Managerlocations: Brazil, São Paulotime type: Full timeposted on: Posted Todayjob requisition id: R-96045At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our...
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Affiliate Pharmacovigilance Manager
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São Paulo, Brasil Eli Lilly and Company Tempo inteiroAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life‑changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...
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Affiliate Pharmacovigilance Manager
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Affiliate Pharmacovigilance Manager
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São Paulo, São Paulo, Brasil Eli Lilly and Company Tempo inteiro R$80.000 - R$120.000 por anoAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...
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Pharmacovigilance Compliance Leader
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São Paulo, Brasil GE HealthCare Tempo inteiroJoin to apply for the Pharmacovigilance Compliance Leader role at GE HealthCare Join to apply for the Pharmacovigilance Compliance Leader role at GE HealthCare Job Description Summary We are seeking a highly motivated and detail-oriented PV Compliance Leader to strengthen our global Pharmacovigilance Quality Team (PV-QA). Job Description Summary We are...
