Clinical Trial Safety Scientist (Pharmacovigilance)

Location: Permanent home-based role in Warsaw, Poland

Annual base pay: PLN 80,500–272,500

Company

Clinical research, healthcare intelligence, and life sciences services supporting the development and commercialization of medical treatments.

What you will do

• Review patient-level clinical and safety data for medical accuracy, completeness, coding consistency, and case closure.
• Generate queries and escalate urgent or critical medical cases to study physicians or medical scientists.
• Prepare aggregated safety data visualizations and facilitate study-level review meetings.
• Support study start-up activities, including document input and tool setup.
• Participate in the Extended Study Team and report on TRISARC deliverables.
• Develop and quality-control automated or handwritten patient narrative processes, and contribute to training and continuous improvement.

Requirements

• Degree in Life Science or equivalent directly related experience.
• At least 2 years of experience in pharmacovigilance or drug safety.
• Understanding of clinical studies and the drug development process.
• Knowledge of ICH/GCP guidelines and SAE reporting requirements.
• Analytical skills, quality focus, and ability to summarize complex information concisely.
• Ability to prioritize multiple deadlines and collaborate cross-functionally on global studies.

Nice to have

• Experience using data review tools.

Culture & Benefits

• Permanent home-based work arrangement.
• Collaboration with internal and external partners across different study phases and therapy areas.
• Health, welfare, and other benefits may be offered depending on the position.
• Incentive plans, bonuses, or other compensation may be available in addition to base pay.