Pharmacovigilance Specialist - Milano, Italia - Sanofi US

Sanofi US

Azienda verificata

Milano, Italia

4 ore fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences.

We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.

Pharmacovigilance Specialist - VIE Contract (W/M):

Target start date: 01/09/2024

As a Pharmacovigilance Specialist you will contribute to the performance of the local Pharmacovigilance activities in compliance with the global policies, as well as global, regional and local Pharmacovigilance regulations to warrant safe and appropriate use of Sanofi products on the market in Italy.

Key responsibilities:

Serve as the Pharmacovigilance Specialist for the products of Sanofi.
Contribution to the maintenance of Pharmacovigilance Operating & Safety Management.
Monitor continuously incoming communication to detect and appropriately manage incoming Pharmacovigilance data to report them in timely manner.
Monitor Pharmacovigilance requirements for global, regional and local programs.
Contribute to the performance of education and training on Pharmacovigilance within the local organization.
Contribute to compliance metrics generation.
Maintain robust collaboration/ interaction with the incountry partner functions.
Identify issues or dysfunction.
Collaborate with regional teams to contribute to the appropriate management of Local Pharmacovigilance system.
Processing Pharmacovigilance data.
Translations of medical texts into English.
Support in the implementation of the Department's current projects.

Key "MUST HAVE" competencies, skills & experiences

Master's Degree in scientific field (Medical Doctor, Pharmacist, Health Sciences, Veterinarian, Biologist or similar).
Minimum 2 years of experience on similar position would be highly preferred.
Knowledge of international and national (pharmacovigilance) regulations as well as industry standards.
Very good knowledge of English is mandatory (good knowledge of medical terminology is additional asset).
Basic knowledge of Italian is mandatory (at least understanding), higher knowledge would be considered as a plus.
Good knowledge of MS Office (Word, Excel, Power Point).
Demonstrate sense of urgency, especially with respect to enforcing safety rules and global procedures as described in Quality Documents, Operational Manuals and Guidance documents.
Ability to work in international and transversal teams.
Interpersonal skills: focus on details, high accuracy in carrying out assigned tasks, perfect organization of work, punctuality, diligence, the ability to set priorities and work under time pressure.

LI-EUR

Pursue _progress_
, discover _extraordinary_**:

Better is out there. Better medications, better outcomes, better science.

But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen.

So, let's be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.