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UDLØBET

Novo Nordisk

Pharmacovigilance Professional

Fuldtid

Permanent

Gladsaxe

SE PÅ KORT
ID: 2569533
|
Indrykket for 20 dage siden

Pharmacovigilance Professional with Strong Data Analysis Skills – Drive Safety Innovations at Novo Nordisk

Are you motivated by performing data analysis, process optimization, and driving projects to ensure high-quality of data? Are you passionate about ensuring the highest standards of quality and safety? Then, this is your moment to take the next step in your professional development in a globally expanding company and become our new Pharmacovigilance Professional.

Apply now for a life-changing career!

The position
As a pivotal figure in our team, your expertise will be channelled into spearheading projects that refine our suite of digital tools (like QlikSense, RPA, and PowerApps). Your capability to transform a multifaceted data environment into critical business insights will be instrumental to our operations.

Other responsibilities will include:

  • Streamlining our quality monitoring processes and guaranteeing the quality of our data. 
  • Contributing to the NextGen Safety project, driving transformative changes in our quality monitoring processes to set the future benchmark in safety standards.
  • Scripting comprehensive User Requirement Specifications (URS) and crafting essential technical documentation.
  • Building robust partnerships across all tiers of our organization is expected, ensuring a seamless exchange between employees and the leadership.
  • Simplifying complex data into actionable insights is at the core of your role. Conveying these insights effectively to our case management team, their management, and other stakeholders is crucial. You will also spearhead root cause analyses to pinpoint problems and devise strategies to maintain data reliability.
  • Qualifications
    To be successful in this role, we are looking for a candidate with the following qualifications:

  • You have a master’s degree in bioinformatics, human biology, biotechnology, medical/pharmaceutical science or similar.
  • Preferable 1-2 years of experience in the pharmaceutical industry.
  • Sharp analytical abilities and a solid understanding of data science, with programming experience being a beneficial addition. 
  • On a personal level, you bring excellent project management and stakeholder engagement skills. Your strong communication abilities enable you to work independently and mesh seamlessly with a team. Curiosity, organization, and an open mind are key aspects of your character.

    About the department
    The Global Safety QC Analysis department is part of the QPPV Office within Global Safety in Novo Nordisk Development. Global Safety is globally responsible for monitoring product safety in Novo Nordisk. 

    The primary responsibility of the QC Analysis department is monitoring the quality of Novo Nordisk product safety information to ensure high data quality to fulfil expectations from regulatory authorities worldwide. We perform trending and analysis based on quality data to identify business needs for procedure updates, and we work closely with case management departments, affiliates, and vendors to align and optimise case management processes and procedures across Global Safety. Our department is digital-first, leveraging an array of advanced digital tools and automation robots to support our many processes. Our dedicated colleagues, based across Denmark and India, work together to achieve our shared goals.

    We offer an exciting job with lots of challenges among good colleagues in a positive, global, and engaging working environment. At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy, and hormone replacement therapy, we offer our employees opportunities for continuous growth.

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