Review, assess, and process safety data and adverse event (AE) reports in compliance with applicable regulations, internal SOPs, and project-specific requirements
Maintain accurate and complete case documentation within pharmacovigilance databases
Code medical terms and products, prepare case narratives, and perform literature surveillance activities as required
Ensure high-quality deliverables and adherence to timelines and productivity targets
Collaborate with cross-functional teams (clinical operations, data management, medical monitors) to resolve safety queries
Participate in audits and inspections, ensuring full compliance with internal and client quality standards
WYMAGANIA:
Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or a related field
Fluent German (primary working language)
Very good command of English (spoken and written)
Knowledge of at least one additional European language (communicative level required)
Strong attention to detail and accuracy in documentation
Familiarity with medical terminology
Proficiency in Microsoft Office
Strong organizational, communication, and problem-solving skills
Ability to work independently and effectively in a fully remote setting within Poland
OFERUJEMY:
Employment contract for 12 months (replacement period)
Fully remote position – work from anywhere in Poland
Competitive salary aligned with market standards
Full onboarding and ongoing professional training
Opportunities for career growth in an international, knowledge-driven environment
