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ID: 2379 Date of Posting: May 9, 2026 Business Area: Pharmacovigilance Job Type: Direct Employee On site / Remote / Hybrid: Hybrid Hub Office: 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.