5 years of progressivelyincreasing clinical research experience within the pharmaceutical/CRO industry preferably in clinical operations in oncology Monitoring experience in oncology clinical trials Experience in management of clinical trials Experience with health authority inspections (FDA and/or EMA) preferred Competencies & Personal Skills Thorough knowledge of drug development regulations (ICH-GCP, FDA, EMA and local regulations)Working experience in a global team, team player Strong interpersonal and leadership skills Excellent problem solving and team building skills Ability to work independently and in a team environment Good organizational and time management skills Ability to work under pressure and meet deadlines Good communication skills Ability to write in a clear, focused and concise manner Fluent in spoken and written English As part of a small high growth business you will get the opportunity to be involved in many different areas and our rapid growth trajectory means you will have the opportunity to grow with us. Nouscom is an equal opportunity employer. We welcome applications from all individuals. We are committed to treating all applicants fairly and avoiding discrimination.

📌 Clinical Study Manager (Roma)
🏢 NOUSCOM
📍 Roma