Pharmacovigilance Specialist

Pharmacovigilance Specialist (Fluent in Portuguese)Pharmacovigilance Specialist (Fluent in Portuguese)Apply locations Buenos Aires, Argentina time type Full time posted on Posted 2 Days Ago job requisition id R1470186Job OverviewReview, assess, and process safety data and information across service lines, received from various sources. Distribute...

Job Description: We are seeking a highly motivated Pharmacovigilance Specialist to join our team at Eddy Pump. As a key member of our Pharmacovigilance department, you will be responsible for SAE case management, including initial case disposition, confirmation of case disposition, receipt of adverse event data, and reporting according to regulatory...

Company OverviewIqvia is a leading provider of advanced analytics, technology solutions, and contract research services to the life sciences industry. Our mission is to help healthcare companies make better decisions that drive human health outcomes.Job DescriptionThe Clinical Data Specialist - Pharmacovigilance will play a critical role in reviewing,...

About the RoleIQVIA Argentina seeks a highly skilled Pharmacovigilance Specialist to join our team. As a key member of our organization, you will play a vital role in ensuring the safety and efficacy of medicines.Main ResponsibilitiesProcess and analyze safety data from various sources, ensuring compliance with regulatory requirements and company...

Job OverviewReview, 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 and support of senior operation team members. This is a...

Job OverviewReview, 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 and support of senior operation team members. This is a...

Job OverviewReview, 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 and support of senior operation team members. This is a...

Job Title: Pharmacovigilance Specialist PVSJob Location: Argentina (In or around the Buenos Aires area)Job Overview: The Pharmacovigilance Specialist (PVS) primary responsibility is SAE case management. This includes but is not limited to initial case disposition, confirmation of case disposition with Medical Monitor (MM)/Safety Physician PV (SP PV), MM,...

Job OverviewWe are looking for a talented Pharmacovigilance Specialist to support our mission of improving patient outcomes. In this role, you will be responsible for reviewing and processing safety data, and collaborating with internal and external stakeholders.Main ResponsibilitiesEnsure that all safety data is processed according to applicable regulations...

Job OverviewWe are seeking a highly motivated Safety Data Specialist to join our team at IQVIA. As a key member of our pharmacovigilance team, you will be responsible for reviewing and processing safety data from various sources.Main Responsibilities:Review and assess safety data from various sourcesDistribute reports and data to internal and external...

IQVIA LLC seeks a skilled Clinical Research Specialist to review, assess, and process safety data across service lines. This role involves distributing reports/data to internal and external parties in compliance with regulations, SOPs, and internal guidelines.Main ResponsibilitiesProcess safety data according to applicable regulations, guidelines, and...

Job SummaryWe are seeking a highly skilled Medical Data Specialist to join our Lifecycle Safety Call Center in Pharmacovigilance. The ideal candidate will have fluency in Spanish, English, and French, with the ability to process safety data according to applicable regulations, guidelines, SOPs, and project requirements.Key ResponsibilitiesProcess and analyze...

We are seeking a detail-oriented Regulatory Compliance Specialist to join our team. In this role, you will be responsible for reviewing and assessing safety data and reports to ensure compliance with regulations and internal guidelines.ResponsibilitiesReview and analyze safety data to ensure compliance with regulations.Distribute reports/data to internal and...

About UsIQVIA Argentina is a leading provider of research and analytics solutions. We are committed to delivering high-quality services to our clients, and we are seeking a talented Pharmacovigilance Specialist to join our team.Main ResponsibilitiesReview and analyze safety data from various sources, identifying trends and patterns.Collaborate with...

Job Summary: We are seeking a talented Pharmacovigilance Specialist to join our team at Eddy Pump. As a key member of our Pharmacovigilance department, you will be responsible for SAE case management, including initial case disposition, confirmation of case disposition, receipt of adverse event data, and reporting according to regulatory requirements.Main...

**Job Summary:**We are seeking a highly motivated and detail-oriented Adverse Event Intake Specialist to join our Pharmacovigilance team at IQVIA.In this critical role, you will be responsible for the accurate and timely intake, processing, and tracking of adverse event reports received from various sources.You will play a vital role in ensuring the safety...

Review, assess, and process safety data and information from various sources.Distribute reports/data to internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines with support from senior team members.Essential Functions Prioritize and complete assigned training on time.Process safety...

Key ResponsibilitiesThis role will involve:Prioritizing and completing assigned trainings on time.Processing safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.Performing Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming...

Job Description:">Highly motivated and detail-oriented individual responsible for the accurate and timely intake, processing, and tracking of adverse event reports received from various sources.Diligently adhere to regulatory guidelines, internal Standard Operating Procedures (SOPs), and global best practices to ensure the safety of products.Perform data...

Job Overview: The Pharmacovigilance Specialist primary responsibility is SAE case management. This includes but is not limited to initial case disposition, confirmation of case disposition with Medical Monitor (MM)/Safety Physician PV (SP PV), MM, receipt of adverse event data, data entry, source document data extraction, draft narrative development,...