Informacje o stanowisku

responsibilities :

• Design, configure, and validate electronic Case Report Forms (eCRF)
• Define data validation and data flow requirements
• Review clinical study protocols and identify data-related requirements
• Ensure completeness, accuracy, and consistency of clinical data in line with the study plan
• Collaborate closely with the clinical research team to clarify study-specific data needs

• Previous experience in a similar role within the medical, pharmaceutical, or biotech industry
• Higher education in medical, pharmaceutical, or life sciences (e.g., pharmacy, chemistry, biology)
• Excellent command of English (written and spoken)
• Strong analytical and communication skills
• Knowledge and understanding of clinical research principles, methods, and standards
• Experience working with digital tools and clinical data management software
• Familiarity with GCP (Good Clinical Practice) and GDP (Good Documentation Practice)

• Opportunity to work in a dynamic, international environment
• Competitive salary and benefit package
• Lunch card
• Private healthcare
• Additional employee benefits

• private medical care
• remote work opportunities
• corporate credit card

Warszawa - Oferty pracy w okolicznych lokalizacjach