Patient Safety Senior Associate

At Novo Nordisk, we strive to create a workplace that values diversity and inclusion. Our Clinical, Medical & Regulatory department is dedicated to ensuring the safety and efficacy of our products. We are seeking a detail-oriented and skilled Senior Patient Safety Associate to join our team.The ideal candidate will have a strong background in patient safety,...

Main Responsibilities As a Patient Safety Senior Associate at Novo Nordisk, you will be responsible for the receipt, documentation, and quality assessment of patient safety information, including adverse events and technical complaints. This involves ensuring compliance with internal and external drug and device safety reporting requirements. Key...

We are seeking a Senior Patient Safety Associate to join our Clinical, Medical & Regulatory department at Novo Nordisk. As a key member of our team, you will be responsible for ensuring compliance with all internal and external drug and device safety reporting requirements regarding the collection and maintenance of safety information.The ideal candidate...

About the RoleAs a Patient Safety Senior Associate at Novo Nordisk, you will be responsible for managing and analyzing safety information, including adverse events and technical complaints. This involves ensuring compliance with internal and external drug and device safety reporting requirements, as well as maintaining accurate records of safety...

About the RoleWe are seeking a highly skilled Patient Safety Senior Associate to join our Clinical, Medical & Regulatory department at Novo Nordisk. As a key member of our team, you will play a vital role in ensuring the safety and efficacy of our products.ResponsibilitiesYou will be responsible for receiving, documenting, triaging, and quality-assessing...

About the RoleAs a Patient Safety Senior Associate at Novo Nordisk, you will be responsible for ensuring the safety and efficacy of our products. This involves receipt, documentation, triage, and quality assessment of inbound safety information, including adverse events and technical complaints. You will also be responsible for ensuring compliance with all...

About the RoleAs a Safety Associate Professional at Novo Nordisk, you will be responsible for managing and assessing safety information related to our products. This includes receipt, documentation, triage, and quality assessment of inbound safety information such as adverse events and technical complaints.You will also ensure compliance with internal and...

About the RoleWe are seeking a highly skilled Drug Safety Associate to join our team at Novo Nordisk in Mexico City. As a key member of the Global Business Service team, you will play a crucial role in ensuring the quality and integrity of our drug safety database.Key ResponsibilitiesEvaluate and classify reported adverse events, ensuring accurate coding and...

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About the RoleWe are seeking a highly skilled Drug Safety Associate to join our team at Novo Nordisk in Mexico City. As a Drug Safety Associate, you will play a critical role in ensuring the safety of our products and maintaining high-quality standards.Key ResponsibilitiesPerform initial evaluation, case entry, and verification of reported adverse events...

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About the PositionNovo Nordisk is a leading global healthcare company with a strong legacy in driving change to defeat serious chronic diseases. We are seeking an experienced Medical Safety Specialist Lead to join our team.Key ResponsibilitiesEnsure compliance with internal and external drug and device safety reporting requirements regarding the collection...