Senior Safety Surveillance Professional
2 days ago
At Novo Nordisk A/S, we are seeking a skilled Safety Surveillance Specialist to join our team.
About the PositionYou will be responsible for establishing and maintaining product safety profiles during development and post-approval phases. This includes conducting safety surveillance of Novo Nordisk products based on worldwide safety information sources.
Establishing and maintaining the product safety profile during development and post-approval phases.
Conducting safety surveillance of Novo Nordisk products during pre-approval and post-approval phases, based on safety information from worldwide sources.
Communicating drug safety issues internally and to health authorities as required.
Chairing or participating in cross-functional safety committees, ensuring effective establishment and execution of meetings.
Taking responsibility for all areas related to patient safety in clinical trials.
To succeed in this role, you must have:
- A master's degree within Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent), complemented by a PhD/research experience.
- Several years of experience within pharmacovigilance and a strong desire to specialize within safety surveillance.
- A solid understanding of medical concepts, scientific methodology, and drug development.
- Excellent communication skills, both written and spoken, with fluency in English.
You should be a team player who thrives in a multicultural and continuously evolving environment. You should also be self-driven and capable of working independently, handling pressure, and meeting tight deadlines in a fast-paced setting.
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