Main Duties & Responsibilities:
*Reporting directly to the Project Manager
*On-site monitoring
*Regulatory and ethics submissions
*In-house monitoring
*Study tracking
*Support of the Trial Leaders and Project Managers
*maximum of 3 visits per week as per contract
Requirements:
*Life science degree (medical or paramedical field is preferred)
*At least 1,5 year experience as a Clinical Research Associate / Monitor in a Contract Research Organization (CRO) or pharmaceutical company
*Good organizational skills with ability to work diligent, accurate and under pressure, alone or as part of a team
*Computer literacy (Microsoft Office Tools)
*Curiosity and willingness to improve skill set
*Good communication skills
*Prepared to travel nationally and internationally
*Fluency in Italian and English, both written and spoken
*Experience in Cardiovascular therapeutic area is an advantage
If you would like to discuss this role in greater details or your application/suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.
We also have a broad variety of other Clinical Research vacancies available in Italy and throughout
For a confidential consultation call Iolanda Oddo on 0044 (0) 207 255 6665 or email your CV to
