Pharmacovigilance & Medical Safety Specialist

Time Personnel; Cape Town; Sur place; ZAR 900 000 - 1 400 000; Plein temps

Résumé du poste

IQVIA invites an Associate Medical Safety Director to lead pharmacovigilance activities across sponsor-dedicated programs. You will provide medical safety oversight, conduct signal detection, and guide risk management for post‑marketing and clinical trial safety reviews.

The role requires an MD with clinical experience and a solid background in pharmacovigilance, regulations, and safety reporting across global portfolios.

Qualifications

• MD with clinical background and pharmacovigilance exposure.
• Experience in signal detection, aggregate reports and risk management.
• Knowledge of global regulatory requirements for safety reporting.

Responsabilités

• Provide aggregate safety reviews and oversight of product safety.
• Lead signal detection and analyses, contribute to safety reports and DA/DSURs.
• Support safety governance meetings and responses to health authorities.

Connaissances

Medical degree

Clinical experience

Regulatory knowledge

Pharmacovigilance

Formation

Medical degree (MD)

Description du poste

IQVIA invites an Associate Medical Safety Director to lead pharmacovigilance activities across sponsor-dedicated programs. You will provide medical safety oversight, conduct signal detection, and guide risk management for post‑marketing and clinical trial safety reviews.

The role requires an MD with clinical experience and a solid background in pharmacovigilance, regulations, and safety reporting across global portfolios.