Pharmacovigilance Medical Safety Lead (Associate)

IQVIA; Ciudad de México; Sur place; MXN 1 800 000 - 3 000 000; Plein temps

Résumé du poste

IQVIA in Mexico City seeks an Associate Medical Safety Director to provide medical expertise across pharmacovigilance services and safety projects. The role requires leading medical reviews, overseeing AOSE analyses, and acting as a consulting safety expert on trials with oversight from senior staff.

The candidate will manage safety content for regulatory reports and participate in client meetings, ensuring timely delivery in a fast-paced environment.

Qualifications

• Medical degree from an accredited medical school.
• 7+ years clinical practice in signal management and safety reporting.
• 9+ years in the pharmaceutical or related industry.
• Knowledge of regulations and guidelines for safety and GCP.

Responsabilités

• Perform medical review of trial-related AEs and ADRs including narrative content, coding, and causality.
• Prepare and review AOSE analyses for expedited cases.
• Provide medical oversight and serve as internal consultant on projects.
• Offer medical safety contributions to Clinical Safety documents and reports.
• Represent safety findings in client meetings and ensure regulatory timelines.

Connaissances

Medical review

Regulatory knowledge

Client facing

Communication

Formation

Medical degree

Medical license

Description du poste

IQVIA in Mexico City seeks an Associate Medical Safety Director to provide medical expertise across pharmacovigilance services and safety projects. The role requires leading medical reviews, overseeing AOSE analyses, and acting as a consulting safety expert on trials with oversight from senior staff.

The candidate will manage safety content for regulatory reports and participate in client meetings, ensuring timely delivery in a fast-paced environment.