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Novo Nordisk A/S, Bagsværd
Is drug safety important to you? Are you excited by digging into information to find answers? Do you want to play a key role in ensuring highest safety and lowest possible risk to patients that use Novo Nordisk products? You may be our new colleague in Safety Surveillance GLP1 Diabetes.
You will be responsible for the ongoing safety surveillance of one or more products used in the treatment of Type 2 Diabetes. This responsibility includes critical analysis and medical evaluation of the emerging safety data, establishment of the product safety profile during development and maintenance of the labelling for marketed products, and communication about the benefit-risk assessment. Once the analysis is done, you will be required to present the data to a group of highly experienced physicians, scientist and managers within the company.
Unique Human Capital recruiting on behalf of Zealand Pharma A/S in Glostrup
An opportunity to contribute to the clinical development of innovative therapies in certain rare diseases and to influence the development of the PV function in a fast growing biotech company
As Senior Specialist Pharmacovigilance at Zealand Pharma you will be part of the department based in Zealand Pharma’s HQ in Glostrup. In collaboration with the Pharmacovigilance Team, you will be responsible for all drug safety related activities for late stage development projects.
With direct report to Senior Director, Head of Pharmacovigilance.
Your main tasks are:
- Development and execution of safety surveillance strategy for assigned clinical projects
- Execution of signal detection activities, to support the evaluation and decisions of Zealand Safety Committee
- Preparation of high quality aggregated periodic safety reports (DSUR, periodic SUSAR reports)
Department of Veterinary Clinical Sciences, Faculty of Health and Medical Sciences at the University of Copenhagen invites applications...
Københavns Universitet, Frederiksberg C