[Hiring] Pharmacovigilance Regulatory Reporting Specialist @IQVIA

Role Description

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

• Reviewing, assessing, and processing safety data and information received from various sources.
• Distributing 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.
• Processing safety data according to applicable regulations, guidelines, SOPs, and project requirements.
• Ensuring compliance with quality, productivity, and delivery standards per project requirements.
• Tracking cases as applicable to the project plan.
• Identifying and reporting quality problems to senior team members.
• Liaising with different functional team members and health care professionals to address project-related issues.
• Attending project team meetings and providing 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)
• Experience 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-based

Company Description

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.