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PV Contract Specialist

ID:  2379
Date of Posting:  Mar 12, 2026
Business Area:  Pharmacovigilance
Job Type:  Direct Employee
On site / Remote / Hybrid:  Hybrid
Hub Office: 

Milano, IT

Territory: 
Full-Time or Part-Time:  Full Time
Seniority:  Mid-senior

With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn.

We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries.

At Recordati, our mantra is simple. We’ve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest – we want to give people the opportunity to be the best version of themselves.

This drive will never stop. Together, we will always be reimagining tomorrow – with new ideas, new technologies and new innovations to fight diseases.

Recordati. Unlocking the full potential of life.

Job Purpose

We are looking for a PV Contract Specialist who cooperates with the Pharmacovigilance Agreements and Budget Group Coordinator in the implementation of PV/Safety Agreements with Contractual Partners and Service Agreements
with PV Service Providers

Key Responsibilities

 Performing, in collaboration with the Pharmacovigilance Agreements and Budget Group Coordinator, all
the activities necessary for the implementation and maintenance, in accordance with the enforced
legislations and Company’s SOPs/Wls of:
 PV Agreements (PVA), including the Transitional Plans (PVTP), with Contractual Partners
 Service Agreements (SA) with the PV Service Providers (e.g. CRO, Vendor, MSSO, WHO)
 PV clause in Quality agreement with manufacturers present in the PIL of Recordati/Italchimici
products
 Materiovigilance Agreements (MVA) for medical devices and any other safety agreement for food
supplements and cosmetics
 Archiving electronically the documentation related to the agreements
 Maintaining the dedicated agreements tracking tables updated

Required Education

Scientific degree 

Master in pharmacovigilance is a plus 

Required Skills and Experience

From 2 to 3 years experience in a PV role

Able to work in a team and problem-solving skills.

Analytical skills

Required Behaviours and Competencies

Required Languages

Good knowledge (written and oral) of the English language is required. Further knowledge of languages is a plus.

At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.

If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.

Apply now »