IQVIA
Pharmacovigilance Specialist
Mexico · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerIQVIA
- LocationMexico
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
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 role requires fluency in English and Spanish.
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.
Show full description
Liaise with different functional team members and healthcare professionals to address project-related issues.
Qualifications
Bachelor’s degree in Life sciences or a related field (mandatory)
Fluency in English and Spanish (mandatory)
Up to 3 years of previous clinical experience (desirable)
1 year of pharmacovigilance experience will be highly valued (desirable)
Work modality:
100% home-based
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
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked