Global Patient Safety Partner — Pharmacovigilance & Impact

Roche; Buenos Aires; Presencial; ARS 1.800.000 - 2.800.000; Jornada completa

Descripción de la vacante

Roche Argentina is seeking a Patient Safety Partner (PSP) to ensure the safe use of medicines by working across functions and maintaining regulatory compliance. This role has direct impact on patient health and offers collaboration both locally and globally in a dynamic environment.

You will monitor local safety profiles, manage adverse events, support audits, and collaborate with Medical, Regulatory, and Clinical teams to implement safety strategies.

Formación

• Hold a degree in Life Sciences or Health-related fields (Pharmacy, Medicine, Public Health, etc.).
• One year of experience in Pharmacovigilance.
• Experience in Regulatory Affairs, Medical Information, or Clinical Operations is valued.
• Knowledge of Argentina regulatory environments for safety, registrations, and renewals.
• Fluency in English to interact with global and regional teams.

Responsabilidades

• Monitor and manage the local safety profile of Roche products and adverse event reports.
• Ensure PV regulations compliance and readiness for audits/inspections.
• Act as safety contact with internal teams, health authorities, and external stakeholders.
• Collaborate with Medical, Access, Health System and Patient Journey Partners on safety strategies.
• Design and execute local safety strategies aligned with global objectives.
• Communicate safety risks and mitigations clearly to healthcare professionals.
• Identify trends and opportunities to enhance patient safety outcomes.

Conocimientos

Pharmacovigilance

Cross-functional collaboration

Regulatory awareness

Fluent English

Educación

Degree in Life Sciences or Health-related fields

Descripción del empleo

Roche Argentina is seeking a Patient Safety Partner (PSP) to ensure the safe use of medicines by working across functions and maintaining regulatory compliance. This role has direct impact on patient health and offers collaboration both locally and globally in a dynamic environment.

You will monitor local safety profiles, manage adverse events, support audits, and collaborate with Medical, Regulatory, and Clinical teams to implement safety strategies.