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Our ever-growing Lifecycle Safety Medical team is expanding. The role participates in all aspects of the Medical Safety activities as per scope of work. This includes, but is not limited to providing and maintaining of PV and risk management expertise to internal and external stakeholders, maintaining knowledge relevant to allocated product portfolios,...

The Qualified Person Responsible for Pharmacovigilance (QPPV) is a mandatory position Marketing Authorization Holders (MAHs) are required to have when operating as entities in the European Union (EU). The QPPV is responsible for the establishment and maintenance of the MAH’s pharmacovigilance system.The Associate Marketed Product Safety director  is...

Who we are Worldline helps businesses of all shapes and sizes to accelerate their growth journey - quickly, simply, and securely. We are the innovators at the heart of the payments technology industry, shaping how the world pays and gets paid. Our technology powers the growth of millions of businesses across 5 continents. And just as we help our customers...

Description The Strategy Business Analyst, based in SCOR’s Bucharest office, supports the Paris-based P&C Strategy team in producing, consolidating, and analyzing the data required for various strategic workstreams. The role spans all pillars of the team’s mandate—Strategic Planning, Business Development, Strategic External Reporting & Messaging,...

At IQVIA, we are committed to advancing healthcare through innovative clinical research. We are currently seeking an experienced Clinical Trials Assistant to join our Sponsor-Dedicated Functional Service Provider (FSP) team in Romania.In this role, you will provide essential support to project teams in the successful execution of clinical trials across a...

PURPOSE Provide administrative support to clinical projects under direction of line manager, Clinical Research Specialist and/or other designated clinical team members. Assists with general administrative functions as required.RESPONSIBILITIES · Assist Clinical Research Specialist (CRS)/In-house Clinical Research Specialist (iCRS), Clinical Research...

At IQVIA, we help life sciences organizations accelerate the development and commercialization of innovative therapies that improve patient outcomes worldwide.We are seeking an experienced Associate Program Director, Regulatory Affairs to join our Global Regulatory Affairs team in Eastern Europe. In this strategic client-facing role, you will lead complex...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Home Based role requiring a RSU with Romanian language...

At IQVIA, our Global Regulatory Affairs team partners with pharmaceutical and biotechnology companies worldwide to navigate complex regulatory environments and accelerate access to innovative therapies.We are seeking an experienced Regulatory Affairs professional with deep expertise in European regulatory affairs and biologic products. This role is ideal for...

At IQVIA, our Global Regulatory Affairs team partners with pharmaceutical and biotechnology companies worldwide to navigate complex regulatory environments and support the successful development, approval and lifecycle management of healthcare products.We are seeking an experienced Regulatory Affairs professional with significant expertise in Advertising &...