Pharmacovigilance Regulatory Reporting Specialist PCD

IQVIA; São Paulo; Remote; BRL 100,000 - 167,000; Full time

Benefits offered by this job

Home-based

Job summary

IQVIA is seeking a Regulatory Reporting Specialist to support submission of safety reports to regulatory authorities. The role involves reviewing safety data, processing information from diverse sources, and distributing reports per SOPs and guidelines, under senior supervision.

The ideal candidate has a life sciences degree, advanced English, 2–3 years in pharmacovigilance, and Argus experience, with strong organizational skills and the ability to work independently or in a team.

Qualifications

• Bachelor's degree in life sciences.
• Advanced level English.
• 2-3 years of experience in pharmacovigilance activities.
• Experience in regulatory reporting is highly valued.
• Previous experience with Argus is required.
• Good knowledge of medical terminology and safety databases.
• Strong organizational skills, attention to detail, and ability to work independently and in a team.

Responsibilities

• Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
• Ensure compliance with quality, productivity, and delivery standards per project requirements.
• Track cases as applicable to the project plan.
• Identify and report quality problems to senior team members.
• Liaise with different functional team members and health care professionals to address project-related issues.
• Attend project team meetings and provide feedback to the operations manager on challenges, issues, or successes.

Skills

English (Advanced)

Pharmacovigilance experience

Medical terminology

Education

Bachelor's degree in life sciences

Tools

Argus

Job description

Job Overview

As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities.

Review, assess, and process safety data and information received from various sources.

Distribute reports/data to 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.

Essential Functions

• Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
• Ensure compliance with quality, productivity, and delivery standards per project requirements.
• Track cases as applicable to the project plan.
• Identify and report quality problems to senior team members.
• Liaise with different functional team members and health care professionals to address project-related issues.
• Attend project team meetings and provide feedback to the operations manager on challenges, issues, or successes.

Qualifications

• Bachelor's degree in life sciences
• Languages: Advanced level of English
• 2-3 years of experience in pharmacovigilance activities (mandatory)
• Specifically in regulatory reporting, will be highly valued.
• Previous experience working with Argus is required
• Good knowledge of medical terminology and applicable safety databases.
• Strong organizational skills, attention to detail, and ability to work independently and as part of a team.

Work modality:100% home-basedIQVIA 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.

Vaga Exclusiva para Pessoa com deficiência (PCD)