Pharmacovigilance Specialist, Adverse Events Intake

**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...

Highly motivated and detail-oriented Adverse Event Case Intake Processor to join our growing Pharmacovigilance team.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 of our products by diligently...

Highly motivated and detail-oriented Adverse Event Case Intake Processor to join our growing Pharmacovigilance team.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 of our products by diligently...

Job Overview:">We are Iqvia Argentina, a leading healthcare company dedicated to improving human health outcomes by providing innovative solutions and services.We are seeking a highly motivated and detail-oriented Adverse Event Case Intake Processor to join our growing Pharmacovigilance team.In this critical role, you will be responsible for the accurate and...

About the Role:">We are seeking a highly motivated and detail-oriented Adverse Event Case Intake Processor to join our growing Pharmacovigilance team.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...

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:">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...

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...

Pharmacovigilance Specialist (Fluent in Italian)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...

The Adverse Event Intake Coordinator plays a critical role in ensuring the timely and accurate processing of adverse event reports related to our company's products.This position is responsible for receiving, reviewing, and processing incoming adverse event reports (AEs) from various sources, including healthcare professionals, consumers, and regulatory...

**Job Overview:**IQVIA is seeking an experienced Pharmacovigilance Case Processor to join our growing team. As a key member of our Pharmacovigilance team, you will be responsible for the accurate and timely intake, processing, and tracking of adverse event reports.This critical role requires a high level of attention to detail, strong organizational skills,...

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,...

IQVIA LLC is seeking an experienced Pharmacovigilance Expert to perform pharmacovigilance activities including collecting and tracking incoming Adverse Events (AEs) and endpoint information. This role requires strong communication skills and the ability to work effectively in a team environment.ResponsibilitiesCollect and analyze safety data from various...

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 DescriptionThe Pharmacovigilance Expert will be responsible for collecting and tracking incoming Adverse Events (AE)/endpoint information, determining initial/update status of incoming events, database entry, coding AE and products, writing narratives, and literature-related activities.ResponsibilitiesProcess safety data according to applicable...

About the Role:The Adverse Event Intake Coordinator plays a critical role in ensuring timely and accurate processing of adverse event reports related to our company's products. This position is responsible for receiving, reviewing, and processing incoming adverse event reports from various sources, including healthcare professionals, consumers, and...

As a Pharmacovigilance Expert at IQVIA LLC, you will play a crucial role in ensuring the safety of drugs on the market. Your primary responsibility will be to review, assess, and process safety data received from various sources. This includes distributing reports/data to both internal and external third parties following applicable regulations, Standard...