노바티스 · RA Specialist

Job Description 4! The 4 essential elements that shape our culture: Inspired. Curious. Unbossed. Integrity. Our mission is to discover new ways to improve and extend peoples’ lives. Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers. With a strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly.We are on our journey to reimagine medicine and our team focus on delivering healthcare solution which fit for purpose. We strive to be the best place to work where our associates could be their best self each day and every day to unleash their full potential. We are looking for individual to join our team who have passion to improve and extend people’s lives. Your Responsibilities: Your responsibilities include, but not limited to:• Support to prepare dossiers for NTO related new products registration & approved products maintenance and support to obtain NTO related approvals from MFDS.• Support the NTO related CTA actions in collaboration with relevant Stake Holders (e.g., medical team, global team, CTA Hub etc.), if required.• Ensure NTO related Novartis compliance with P3, KRPIA code of conduct, relevant regulations and laws for related CPO activities (DRAGON update, RMP, artwork, barcode, Drug ID mark, promotional materials/activities, PMS/drug safety reporting etc.).• Ensure reporting and follow up of all spontaneous adverse events (AE) and technical complaints for all Novartis products according to respective SOP• Any other NTO related RA activities, if needed Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients

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