At Novo Nordisk we don't wait for change, we drive the change. We're committed to promote and be an equal opportunity workplace and act as an affirmative action employer, as part of our continuous efforts to create and lead teams that have diversity and inclusion at their core.We are looking for a Senior Patient Safety Associate to join our Clinical, Medical & Regulatory department at Novo Nordisk.If you are detail-oriented, have strong communication skills, and committed to compliance, then read on and apply today for a life-changing career.Join Novo Nordisk for a life-changing career establishing and developing a world-class Global Business Service Centre in Mexico City.The positionAs a Patient Safety Senior Associate at Novo Nordisk, you will be responsible for receipt, documentation, triage and quality assessment of inbound safety information, including adverse events and technical complaints.Also responsible for ensuring compliance with all internal and external drug and device safety reporting requirements regarding the collection and maintenance of safety information.Along with that you will :Duplicate searches, Product Coding and Narrative Generation.Handling inbound and outbound calls and correspondence for adverse events and technical complaints, providing professional and timely responses to product information questions and inquiries.Assist with training and mentoring of new joiners and assist with workload distribution and coordination.Identify opportunities of development of the procedures and make recommendations to management and support implementation of solutions.QualificationsBachelor's degree in a science or healthcare discipline.3+ years of patient safety experience, preferably with customer service experience.Strong knowledge of medical and pharmacovigilance terminology.Experience with MedDRA coding and adverse event identification is preferred.It will be considered as an asset if you have knowledge and experience with disease states supported by Novo Nordisk, such as diabetes, obesity, haemophilia, and growth hormone disorders.You have Advanced or Fluent Level of Spanish and English.Familiarity with FDA regulations, computer validation, and Sarbox regulatory requirements.Proficiency in test case writing and execution is a must.About the departmentThe Clinical, Medical & Regulatory department at Novo Nordisk is dedicated to ensuring the safety and efficacy of our products.We work closely with healthcare professionals, patients, and regulatory authorities to collect and analyse safety information.#J-18808-Ljbffr
