Senior Safety Surveillance Analytical Professional (1 year contract)
at Novo Nordisk
Søborg, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 04 Feb, 2025 | Not Specified | 23 Jan, 2025 | 3 year(s) or above | Pharmacovigilance | No | No |
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Description:
Senior Safety Surveillance Analytical Professional (1 year contract)
Category: Reg Affairs & Safety Pharmacovigilance
Location:Søborg, Capital Region of Denmark, DK
Are you passionate about ensuring the safety of medicines? Do you want to play a cru-cial role in safeguarding patients? We are looking for a Senior Safety Surveillance Pro-fessional to join our team on a 1-year contract in Denmark. If that sounds like you, read on and apply today for a life-changing career.
THE POSITION
We are currently seeking a Senior Safety surveillance Analytical Professional to help drive a range of analytical projects. We promise a dynamic and rewarding experience at a leading global healthcare company - Novo Nordisk. As an experienced Safety Surveil-lance analytical Professional, you will play an important role in a wide variety of tasks and activities such as providing surveillance requirements into projects, providing input into data analysis strategies for signal detection and signal validation, and driving im-provement processes.
As a Senior Safety Surveillance Analytical Professional at Novo Nordisk, you will:
- Co-develop and implement data analysis strategies that align with Safety Surveillance objectives and data sources
- Act as an application owner for analytical, signal, and risk detection tools
- Be responsible for training of analytical, signal and risk tracking tools within Safe-ty Surveillance
- Be responsible for providing safety surveillance requirements for the safety and clinical databases
- Participate in project activities to enhance signal detection processes and risk management
- Perform complex ad hoc analysis requests from end users or Health Authorities
- Collaborate closely with colleagues and stakeholders to resolve IT tools inci-dents/deviations in Safety Surveillance.
QUALIFICATIONS
- PhD, Masters, Bachelor or equivalent in natural science.
- PhD with 3-4 years relevant experience, master’s with 5-7 years relevant experi-ence, Bachelor with 8-11 years relevant experience or equivalent knowledge through relevant practical experience.
- Experience in signal detection/pharmacovigilance
- Shows curiosity and a learning mindset towards yourself and processes
- Builds and maintains stakeholder relations globally
- Shows ability and willingness to quickly adjust to new situations in a continuously developing environment.
- Shows ability to manage variable workload and ability to plan and coordinate tasks – can manage many projects at the same time
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:3.0Max:11.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Phd
Proficient
1
Søborg, Denmark