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Pharmacovigilance Coordinator | São Paulo – Join Roche to contribute to a healthier future by preventing, stopping and curing diseases. We celebrate individuality, encourage open dialogue, and value every voice at Roche. The Position A healthier future motivates us to innovate. As a PV Coordinator you’ll support the implementation, maintenance and oversight of the local PV system for the assigned affiliate(s)/country(ies). Your focus is ensuring an efficient and effective PV system that complies with global Roche and local legal/regulatory authority PV requirements, safeguarding our License to Operate. Support the execution of IPS & Affiliate’s Patient Safety (APS) strategies, ensuring high‑quality implementation both locally and globally, while demonstrating leadership in ownership, collaboration, and decision‑making within assigned responsibilities. About the Opportunity Collaborate with the execution, implementation, maintenance, and oversight of the local PV system. Manage key safety‑related activities in line with Roche procedures. Act as the primary safety expert and trusted point of contact for Global Safety, PV Hubs, and local field teams (PJPs/HSPs) within the assigned Therapeutic Area. Represent and lead PV‑related projects and decisions in cross‑functional teams. Co‑create, drive, and implement the local Patient Safety strategy, anticipating unmet needs and aligning global strategies with local business priorities and new launches. Collaborate closely with cross‑functional partners (Medical, Access, PJP/HSP) to ensure the safety strategy is integrated into the overall disease area plan. Actively contribute ideas and expertise to local and above‑country projects, sharing experiences and best practices that benefit the network. Influence to gain support for initiatives from cross‑functional teams and build trusting relationships with internal stakeholders. Engage in horizon scanning to identify emerging trends and opportunities, helping to accelerate and scale innovative Patient Safety solutions. Who you are Bachelor’s degree in Life Sciences or a related health discipline. Advanced proficiency in English. Desired at least 5 years of experience in PV, particularly in an affiliate setting. Managed projects with a higher level of complexity, cross‑functionally or cross‑border. Understanding the affiliate PV System to be the decision maker for the department in cross‑functional meetings. Desired experience in other affiliate medical functions (e.g., Regulatory Affairs, Medical Information, Clinical Operations, Medical Affairs) or global clinical product development/clinical safety is considered advantageous. Strong experience and expertise in Pharmacovigilance and deep understanding of how decisions are made in the local & Global PV ecosystem. Solid understanding of drug development, the pharmaceutical industry, and local regulatory requirements. Deep understanding of the local environment and proven ability to build trusting relationships and influence cross‑functional teams. Strategic mindset, systems thinking, critical thinking skills, and outcome‑based planning. Customer‑centric mindset with strong understanding of patient journeys, health systems, and Roche products. Availability to work in a hybrid model based in São Paulo. Relocation benefits are not available for this position. Roche is an Equal Opportunity Employer. Seniority level Mid‑Senior level Employment type Full‑time Job function Research, Science, and Engineering Industries Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing #J-18808-Ljbffr
