We are currently looking for a Clinical Trial Assistant to join our multi-sponsor team in Milan.
As a CTA with IQVIA, you will be responsible for providing administrative support to clinical projects under direction and supervision of line manager and / or other designated clinical team members.
Assist Clinical Research Associates (CRAs) / and Regulatory and Start-Up Specialists (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines
Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
Assist with periodic review of study files for completeness
Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information
Assist with payment process to Hospital Administration
Assist with update of Regulatory Database
Desired Skills and Experience
MSc degree with strong record of academic achievement, preferably in Scientific / Life Science field (Pharmacy, CTF, Biology, Chemistry etc.)
At least 1-2 years of experience in similar positions
Good understanding of clinical trial processes
Proficiency both in English (written and spoken) and Italian
Excellent Microsoft Office Skills
Good communication skills
Ability to be multi-tasking in a fast paced environment and to work on a team