Lublin, lubelskie

Pharmacovigilance Specialist


  • Processing adverse events information in a global database based on source data using medical knowledge
  • Quality control of entered data, ensuring consistency and compliance with formal requirements
  • Substantive cooperation with international teams in order to ensure the highest quality of reporting and work efficiency
  • Participation in projects increasing the innovation of the Safety and Clinical Data Management Services

We offer:

  • Stable employment contract
  • Open for candidates across Poland (remote/hybrid working model, company support in relocation)
  • Great atmosphere within innovative team and empowering environment to share ideas
  • Peer Buddy Mentor introducing you to the organization
  • Medical care package, sport card and other attractive benefits


  • University degree in the field of medicine, pharmacy, nursing, veterinary, dentistry, obstetrics, medical analytics, physiotherapy, medical biology, biotechnology, bioinformatics

  • Very good written and spoken English language (B2-C1 level), particularly in usage of medical terminology (verified during recruitment)

  • Very good written and spoken Polish

  • Computer literacy and ease of learning new computer systems and applications

  • High level of organizational skills, ability to follow procedures, good time management and ability to set priorities

  • Ability to solve problems, person with high analytical skills and detail-oriented who can work independently, ready to adequate feedback reception

  • Ability to go extra mile and create friendly working atmosphere based on mutual respect

Please apply as soon as possible via “Apply” button and attach your CV in English/Polish. We screen the applications continuously.


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