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Pharmacovigilance Specialist

  • Sweden
  • Sweden

We are growing, grow with us!
Are you eager to work in a dynamic company where new challenges and opportunities are part of your everyday life? PharmaLex is one of the leading service providers for the worldwide pharmaceutical industry in regulatory affairs, pharmacovigilance, and development consulting.

In the Nordics we are looking for motivated, committed candidates to join our Swedish Pharmacovigilance team.

Your Job

The responsibilities will be dependent on the candidate previous experience, but will be within one or more areas as follows:

  • General guidance (consultancy) of customers regarding pharmacovigilance regulations and handling
  • Plan, Set-up and maintain global pharmacovigilance systems
  • Management of adverse drug reactions from marketed products and clinical trials, including receipt, data entry, review, and reporting of cases
  • Production and review of periodic safety re-ports and risk management plans
  • Literature search
  • Medical information activities, including intake and follow up of adverse events, product enquiry and complaint handling from Swedish patients and healthcare professionals

Skills & Requirements

We are looking for people who have experience working within Pharmacovigilance and meets the additional requirements.

  • Academic degree in pharmacy or life science
  • Well organized and sense of accuracy
  • Service minded, flexible, and committed to meeting deadlines
  • Fluency in spoken and written Swedish and English language
  • Team player
  • Computer literacy and confidence with business applications

About the company

PharmaLex is one of the leading service companies for the pharmaceutical industry globally and is specialized in all aspects of drugs and medical devices approval, of the development to market and any action of effective product maintenance. PharmaLex values includes international mindset, growth & learning, collaboration, quality focus, dynamic working approach and integrity & respect.


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