Senior Medical Safety Director – Lifecycle PV

IQVIA; Lisboa; Presencial; EUR 90 000 - 120 000; Tempo integral

Resumo da oferta

IQVIA is seeking an Associate Medical Safety Director to join our Lifecycle Safety Medical team in Lisbon. You will contribute to medical safety activities, including PV expertise, risk management, and responses to health authorities, across product portfolios and studies.

The role requires a medical degree and about three years of clinical practice plus industry exposure, strong ability to synthesize data, and collaboration with global stakeholders.

Qualificações

• A medical degree from an accredited and internationally recognized medical school.
• Around three years of clinical practice experience with two additional years in the pharmaceutical or associated industry, or equivalent combination of education, training and required experience.
• Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice and clinical trials and pharmaceutical research process.
• Maintain knowledge of assigned product portfolio, therapeutic area, and recent literature.
• Experience in Signal detection, Aggregate reports and Risk management.
• Capability to synthesize and critically analyze data from multiple sources and communicate complex clinical issues and analyses orally and in writing.

Responsabilidades

• Providing aggregate reviews of safety information to maintain oversight of a product’s safety profile.
• Leads signal detection and analysis, including signal detection strategy, frequency, and timing; reviews reports and data; raises potential signals for discussion.

Conhecimentos

Medical safety

Signal detection

Pharmacovigilance

Medical review

Regulatory knowledge

Formação académica

Medical degree

Descrição da oferta de emprego

IQVIA is seeking an Associate Medical Safety Director to join our Lifecycle Safety Medical team in Lisbon. You will contribute to medical safety activities, including PV expertise, risk management, and responses to health authorities, across product portfolios and studies.

The role requires a medical degree and about three years of clinical practice plus industry exposure, strong ability to synthesize data, and collaboration with global stakeholders.