Hobson Prior are currently looking for a Pharmacovigilance Specialist, Case Management to join a brilliant pharmaceutical organisation on a permanent basis located in Milan with hybrid working available. Our client is focused on improving human health through distributing regulatory compliance services for the safe and efficient use of medical solutions.

Please note that to be considered for this role you must have the right to work in this location.

Requirements:

• At least 2-6 years of experience within pharmacovigilance, case management and clinical trial, ideally someone with at least 3 years of work experience in a junior role.
• Know-how of EU GVP, ICH and WHO regulations.
• Educated to a degree level in a life science, pharmacy or medicine discipline.
• Knowledge of case management of post marketing ICSRs such as consumer, doctor literature, regulatory etc.
• Knowledge of case management of clinical trial such as phase II, III, etc.
• Comprehension of 15 days and 90 days reporting of all cases.
• Familiarity with any one of the safety databases: Argus, Aris G, AB cube, Veeva, etc.
• Comprehension of serious/non-serious case and SUSAR.
• At least 1-2 years of experience in MedDRA coding and narrative writing.
• At least 1-2 years of experience within data entry, triaging of cases, and following up on case requests.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.