Offer summary
Qualifications:
Degree in scientific or healthcare discipline, Fluent in English and Polish, Minimum 3 years in pharmaceutical industry, 1+ years field monitoring experience, Knowledge of GCP/ICH, FDA, EMA.Key responsabilities:
- Manage assigned study sites and protocols
- Conduct site training and continuous monitoring
- Identify deficiencies and implement improvements
- Collaborate with internal stakeholders for data quality
- Perform site closeout activities and documentation