Informacje o stanowisku

ZAKRES OBOWIĄZKÓW: - 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

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