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)
• Entering business growth opportunities, training and mentoring programs related to clinical trials and soft skills
• 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:

• 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

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