Associate, Drug Safety DACH (f/m/d)

  • Full-time
  • Region: EU+/Canada
  • Department: Quality

Qualifications

For our Munich office (in a hybrid working model) we are recruiting for an

Associate, Drug Safety DACH (f/m/d)

in temporary employment via 3rd party.

The position will be responsible to support all relevant PV activities within the DACH region. This includes but is not limited to routine activities as reconciliation activities, triage of cases, follow-up letters and other compliance related documentations. In addition, the role will support the international pharmacovigilance team in all administrative tasks and documentation related to Safety report intake and reconciliation to support a global database transfer project. 

What You’ll Do

Drug Saftey:

  • Conducting and documenting of PV Intake related activities
  • Mailbox screening
  • Reconciliation and quality related activities
  • Supports Drug Safety team in collecting, documenting, and processing of adverse event and pregnancy reports.
  • Performs affiliate triage of incoming safety reports incl. triage based on seriousness.
  • Supports Drug Safety team in management and tracking of follow-up requests 

Global Database Project Management: 

  • Administrative planning and monitoring of project related tasks
  • Support of data transfer and local database (VAST) related activities as part of the global database project
  • Support on project related activities as needed

Who You Are

You are an open and dynamic person, ready to grow and succeed in a complex environment. You are always striving to challenge the status quo as well as to optimize existing processes and procedures.

 

Additional Information

Required Skills

  • Degree in natural sciences or equivalent education in combination with initial professional experience in a scientific department of the pharmaceutical industry
  • Preferred:  3 years of experience in Pharmacovigilance or comparable fields (e.g. Quality)
  • Project management experience beneficial
  • Database handling
  • Excellent skills with MS Office applications
  • Ability to work in complex cross functional teams
  • Knowledge of GDP and European Pharmacovigilance legislation 
  • English and German language skills

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

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