Patient Safety Senior Associate
hace 1 semana
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 will have a strong knowledge of medical and pharmacovigilance terminology, as well as experience with MedDRA coding and adverse event identification. Additionally, proficiency in test case writing and execution is a must.
About the role:
- Receipt, documentation, triage and quality assessment of inbound safety information, including adverse events and technical complaints.
- 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.
About the department:
The 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.
About Novo Nordisk:
Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily.
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Patient Safety Senior Associate
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