Safety Data Analyst

4 days ago


Solna Municipality, Sweden Allergan Full time

**Role Overview**

A Drug Safety Manager plays a critical role in ensuring the safety of AbbVie's products by identifying, evaluating, and reporting adverse events. As a key member of the Scandinavia Pharmacovigilance & Medical Info team, you will be responsible for managing Adverse Event reports, conducting quality checks, and educating colleagues and external partners on pharmacovigilance best practices.

  • Responsibilities include reviewing and processing Adverse Event reports, conducting quality checks, and providing training to new PV staff/contractors. You will also collaborate with cross-functional teams to ensure alignment with business objectives and regulatory requirements.
  • Develop and maintain effective relationships with internal stakeholders, including Sales, Marketing, and Regulatory Affairs.
  • Stay up-to-date with regulatory requirements and industry trends in pharmacovigilance.
  • Identify opportunities for process improvements and implement changes to enhance efficiency and effectiveness.
  • Contribute to the development of policies and procedures related to pharmacovigilance.

The ideal candidate will have a strong understanding of pharmacovigilance principles and regulations, as well as excellent communication and interpersonal skills.


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