Senior Pharmacovigilance & Aggregate Reports Lead

Anonymous; South Africa; On-site; ZAR 700,000 - 1,000,000; Full time

Job summary

IQVIA in South Africa is seeking a Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2) to lead signal detection and literature safety surveillance on marketed and investigational products. You will author and finalize aggregate reports, respond to regulatory inquiries, and oversee molecule deliverables within a cross-functional team, ensuring timeliness and compliance.

This full‑time, on‑site role requires 4–6 years of pharmacovigilance experience, excellent English

Qualifications

• 4-6 years of pharmacovigilance experience
• Experience with aggregate reports and signal management
• Excellent written and verbal English communication
• Ability to work effectively in a team
• Healthcare background preferred

Responsibilities

• Act as signal detection and literature lead for safety surveillance.
• Author and finalize aggregate reports (PBRERs/PSUR/DSURs/ACOs).
• Respond to regulatory inquiries as required.
• Coordinate molecule work and KPI compliance across teams.
• Lead SD/Lit meetings and QA of deliverables.
• Ensure timely completion of molecule deliverables and proper documentation.
• Participate in audits and training to maintain compliance.

Skills

Pharmacovigilance experience

Drug safety knowledge

Signal detection

Communication skills

Teamwork

English fluency

Education

Life science degree or related

Job description

IQVIA in South Africa is seeking a Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2) to lead signal detection and literature safety surveillance on marketed and investigational products. You will author and finalize aggregate reports, respond to regulatory inquiries, and oversee molecule deliverables within a cross-functional team, ensuring timeliness and compliance.

This full‑time, on‑site role requires 4–6 years of pharmacovigilance experience, excellent English