Pharmacovigilance Specialist
hace 2 semanas
Pharmacovigilance Specialist (Operations Specialist 2) 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 #J-18808-Ljbffr
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Sr Pharmacovigilance Specialist
hace 6 días
Municipio de Rincón de los Sauces, Argentina IQVIA A tiempo completoSr Pharmacovigilance Specialist (Operations Specialist 2) Join to apply for the Sr Pharmacovigilance Specialist (Operations Specialist 2) role at IQVIA. 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...
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Pharmacovigilance Analyst
hace 6 días
Municipio de Rincón de los Sauces, Argentina Cognizant A tiempo completoJob Summary Join our dynamic team as a Pharmacovigilance Specialist where you will play a crucial role in ensuring the safety and efficacy of pharmaceutical products. With a focus on Pharma Research & Development you will contribute to the monitoring and evaluation of drug safety data. This hybrid role offers a balanced work environment with no travel...
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Senior Pharmacovigilance Ops Specialist
hace 6 días
Municipio de Rincón de los Sauces, Argentina IQVIA A tiempo completoA global leader in clinical research services is seeking a Sr Pharmacovigilance Specialist to work from home in Neuquén, Argentina. The successful candidate will handle safety data processing and mentor junior staff while ensuring compliance with regulations. A bachelor's degree in life sciences and advanced English skills are mandatory. The role promises a...
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Remote Pharmacovigilance Specialist — Operations
hace 2 semanas
Municipio de Rincón de los Sauces, Argentina IQVIA A tiempo completoA leading global clinical research firm is seeking a Pharmacovigilance Specialist for a home-based role. You will utilize your expertise to review and process safety data, ensuring compliance with regulations. The ideal candidate will hold a Bachelor's degree in life sciences and possess up to 5 years of relevant experience, including knowledge of ARGUS...
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Hybrid Pharmacovigilance Analyst
hace 6 días
Municipio de Rincón de los Sauces, Argentina Cognizant A tiempo completoA global leader in technology solutions is seeking a Pharmacovigilance Specialist to ensure the safety and efficacy of pharmaceutical products. This hybrid role requires expertise in Pharma Research & Development, focusing on drug safety data monitoring and evaluation. The ideal candidate will possess analytical skills and a relevant scientific degree,...
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Pharmacovigilance Analyst
hace 2 semanas
San Miguel de Tucumán, Argentina Cognizant A tiempo completoJob Summary Join our dynamic team as a Pharmacovigilance Specialist where you will play a crucial role in ensuring the safety and efficacy of pharmaceutical products. With a focus on Pharma Research & Development you will contribute to the monitoring and evaluation of drug safety data. This hybrid role offers a balanced work environment with no travel...
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Pharmacovigilance Specialist
hace 2 días
Municipio de Esquel, Argentina IQVIA A tiempo completoPharmacovigilance Specialist (Fluent in German/French) Job Overview Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance...
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Hybrid Pharmacovigilance Analyst
hace 2 semanas
San Miguel de Tucumán, Argentina Cognizant A tiempo completoA leading pharmaceutical company is seeking a Pharmacovigilance Specialist in San Miguel de Tucumán. In this hybrid role, you will be crucial in ensuring drug safety and efficacy while collaborating with cross-functional teams. The ideal candidate will have a relevant scientific degree and experience in Pharma Research & Development. Strong analytical...
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Regulatory Submissions Specialist
hace 4 semanas
Municipio de Esquel, Argentina IQVIA A tiempo completoOverview Regulatory Submissions Specialist (with Portuguese) This role requires working on National Holidays and weekends as needed. Responsibilities Process safety data according to applicable regulations, guidelines, SOPs, and project requirements. Review, assess, and process safety data and information from various sources. Distribute reports/data to...
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Municipio de Esquel, Argentina Syneos Health A tiempo completoSafety & PV Ops Specialist II - Technology Support (ARGUS Console or Veeva Safety preferred) Direct message the job poster from Syneos Health Overview Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes...
