Offer summary
Qualifications:
Degree in scientific or healthcare discipline, Fluent in written and spoken English and Polish, Minimum 3 years of pharmaceutical industry experience, 1+ years field monitoring experience required, Knowledge of international standards (GCP/ICH, FDA, EMA).
Key responsabilities:
- Manage assigned study sites and phase I-IV protocols
- Perform site initiation and continuous monitoring activities
- Identify deficiencies and work on process improvements
- Ensure adherence to protocol and regulatory compliance
- Collaborate with internal stakeholders for data quality