2 English-speaking jobs in Zamość

Clinical Research Nurse coordinates and conducts studies adhering to GCP, ICH-GCP, and MHRA requirements. Responsibilities include direct participant care, administering IMPs, monitoring adverse events, and maintaining accurate study documentation. Requires RN qualification and NMC registration.

Sub Investigator ensures patient clinical safety and collects accurate data for clinical trials. Responsibilities include leading study teams, managing trials per protocol and GCP, and coordinating regulatory documents. Must be a licensed MD, DO, NP, or PA with 5+ years of experience.