Offer summary

Qualifications:

Bachelor’s degree in life sciences or a related field., Up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience., Fluency in English, Spanish, and Portuguese..

Key responsabilities:

Process safety data according to applicable regulations, guidelines, and SOPs.

Perform pharmacovigilance activities, including tracking Adverse Events and database entry.

Liaise with team members and healthcare professionals to address project-related issues.

Mentor new team members and support department initiatives as assigned.

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com.

Job description

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 and support of senior operation team members. This is a trilingual role requiring fluency in English, Spanish, and French.

Main Responsibilities

Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.
Ensure compliance with quality, productivity, and delivery standards per project requirements.
Liaise with different functional team members and healthcare professionals to address project-related issues.
Mentor new team members and support department initiatives as assigned by the manager.

Qualifications

Bachelor’s degree in life sciences or a related field.
Up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience is valuable.
Fluency in English, Spanish, and Portuguese.

#LI-REMOTE

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 https://jobs.iqvia.com

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