Requirements: English
Company: Antal Pharma & Medical Devices
Region: Warsaw , Masovian Voivodeship
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
requirements-expected :
- 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)
offered :
- Opportunity to work in a dynamic, international environment
- Competitive salary and benefit package
- Lunch card
- Private healthcare
- Additional employee benefits
benefits :
- private medical care
- remote work opportunities
- corporate credit card