International Pharmacovigilance

4 semanas atrás


Lisboa, Portugal Manpower Tempo inteiro

Manpower, the world leader in Human Resources, is currently recruiting an International Pharmacovigilance (IPV) Affairs Associate Manager (M/F) for a prestigious client.

PRINCIPAL RESPONSIBILITIES:

- The IPV Affairs Associate Manager will support the Global IPV Affairs Team in all IPV operational and compliance tasks related to the vigilance of the J&J product portfolio under the umbrella of International Pharmacovigilance (IPV).
- The IPV Affairs Associate Manager will work in close partnership with Regional Heads, Local Safety Teams and Case Management Team to ensure adequate centralization of activities enabling process optimization and increasing efficiencies.
- The IPV Affairs Associate Manager will ensure a consistent operations approach across the regions in alignment with the Global Medical Safety (GMS) and Global Medical Organization (GMO) processes for areas of responsibility.
- The IPV Affairs Associate Manager in partnership with IPV Affairs Project Lead will lead or participate in global or regional multi-disciplinary projects and shape strategies for the projects assigned.

**EDUCATION & EXPERIENCE REQUIREMENTS**:

- Medical, pharmaceutical or nature science degree with proven expertise and experience in pharmaceutical industry and experience in Pharmacovigilance
- Minimum of 1 years’ experience in a position within Pharmacovigilance. 6-8 years related experience.
- Excellent stakeholder management, negotiation skills and coaching people in influencing internal and external partners
- Task-oriented with proven experience in the delivery of high-quality work as part of a multi-disciplinary team
- In-depth understanding of vigilance systems and processes; knowledge of or experience with International Pharmacovigilance and compliance regulations and guidelines is an advantage for this role.
- Demonstrable insight to the development of regulatory requirements with knowledge of Global aspects of drug/cosmetics/devices safety, including international reporting requirements and relevant country-specific variations.
- Fluent communication skills in English, any additional language is a plus

**Location & Travel**

Global Office based role from any Pharma office in the correspondent region. Remote work possible. Up to 25% travel might be required

**Tipo de oferta**: Período Integral

Horário de trabalho:

- Turno de 8 horas



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