Senior Pharmacovigilance Scientist – Aggregate Reports

Badger Holdings; Cape Town; On-site; ZAR 700,000 - 900,000; Full time

Job summary

IQVIA is seeking a Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2) to join our global life sciences team in South Africa. This full-time role focuses on signal detection, aggregate reporting, and cross-functional collaboration across molecule teams and regulatory inquiries.

The ideal candidate has 4–6 years in pharmacovigilance, strong communication skills, and fluency in English. You will contribute to high-quality safety deliverables while adhering to SOPs and quality

Qualifications

• Pharmacovigilance experience in drug safety and aggregate reports.
• Excellent written and verbal communication.
• Ability to work in cross-functional teams and across locations.
• English fluency, both written and spoken.

Responsibilities

• Lead signal detection and literature surveillance.
• Author and finalize PBRERs/PSURs and DSURs.
• Respond to regulatory inquiries as required.
• Coordinate end-to-end molecule deliverables with cross-functional teams.
• Support audits and ensure SOP compliance.

Skills

Pharmacovigilance

Communication skills

Team collaboration

English fluency

Education

Life science degree / pharmacy or related field

Job description

IQVIA is seeking a Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2) to join our global life sciences team in South Africa. This full-time role focuses on signal detection, aggregate reporting, and cross-functional collaboration across molecule teams and regulatory inquiries.

The ideal candidate has 4–6 years in pharmacovigilance, strong communication skills, and fluency in English. You will contribute to high-quality safety deliverables while adhering to SOPs and quality