Operations specialist - Pharmacovigilance

IQVIA Inc; United States; À distance; USD 65 000 - 90 000; Plein temps

Avantages offerts par ce poste

Remote work

Résumé du poste

IQVIA Inc is seeking a bilingual (English/Spanish) Pharmacovigilance Associate to review and process safety data across service lines. You will distribute reports to internal teams and external partners under guidance from senior operations staff.

The role is 100% home-based and requires adherence to SOPs and regulatory guidelines. The ideal candidate has a Life Sciences degree, 1–2 years PV experience, and familiarity with safety databases like ARGUS.

Qualifications

• Bachelor’s degree in Life sciences or related field is mandatory.
• Fluency in English and Spanish is mandatory and will be evaluated.
• 1–2 years of pharmacovigilance experience is valued.
• Experience with Safety Databases (ARGUS or others) is valued.

Responsabilités

• Process safety data according to regulations, SOPs, and project requirements.
• Perform pharmacovigilance activities including AE collection, coding, narratives, and literature tasks.
• Ensure compliance with quality, productivity, and delivery standards.
• Liaise with cross-functional teams and healthcare professionals on project issues.

Connaissances

Bilingual English/Spanish

Pharmacovigilance mindset

Formation

Bachelor’s degree in Life sciences or related field

Outils

ARGUS or equivalent

Description du poste

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 role requiring 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.
• 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) (will be evaluated)
• 1 or 2 years of pharmacovigilance experience will be highly valued (desirable)
• Experience with Safety Databases will be highly valued (ARGUS or others) (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.