Pharmacovigilance Specialist
Duties:
- 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
Requirements:
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University degree in the field of medicine, pharmacy, nursing, veterinary, dentistry, obstetrics, medical analytics, physiotherapy, medical biology, biotechnology, bioinformatics
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Very good written and spoken English language (B2-C1 level), particularly in usage of medical terminology (verified during recruitment)
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Very good written and spoken Polish
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Computer literacy and ease of learning new computer systems and applications
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High level of organizational skills, ability to follow procedures, good time management and ability to set priorities
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Ability to solve problems, person with high analytical skills and detail-oriented who can work independently, ready to adequate feedback reception
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Ability to go extra mile and create friendly working atmosphere based on mutual respect