Senior Safety Surveillance Analytical Professional (1 year contract)

at  Novo Nordisk

Søborg, Region Hovedstaden, Denmark -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate04 Feb, 2025Not Specified23 Jan, 20253 year(s) or abovePharmacovigilanceNoNo
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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