CRAcademy internship - Clinical Department

Do you want to transform Clinical Trial World? IQVIA is developing new ways to drive clinical trials forward! This is a great moment to join us!

Are you interested in starting your career in clinical research field within a multinational company?

We are currently looking for interns to join our Clinical Operations team based inMilan.

As an intern with IQVIA, you will have the possibility to deepen your knowledge of the clinical world as part of one of the biggest CRO in the world.

Under the direction and supervision of line managers and colleagues, you will have the possibility to gain a complete overview on how clinical trials are managed by supporting the activities of different teams (such as CRAs/CTAs/RSUs).

We offer a full training program with class sessions (managed by experienced line managers) and practical trainings;  you may have the possibility to perform on site and remote monitoring activities shadowing experienced Monitor with, at the end of the program, the possibility to receive the CRA Certification (as prescribed by DM 2011/15) directly by IQVIA!

During your internship within IQVIA you will have the possibility to:

• Be trained on clinical research world and IQVIA’s methodology;

• Be familiar with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information;

• Collaborate on projects related to CRA activities, deepen your knowledge in the type of activities that CRA usually deal with (internal data record systems, interaction with sites etc);

• Assist IQVIA’s professionals (CRAs/CTAs /RSUs) in accurately updating and maintaining clinical systems that track site compliance and performance within project timelines;

• Support IQVIA’s professionals (CRAs/CTAs /RSUs)in the maintenance of the study documentation;

• Be responsible for providing support to clinical projects under direction and supervision of line manager and/or other designated clinical team members (also starting a direct interaction with sites and clients)

Your rewards:

• Career & development opportunities - we are the leader CRO, opportunities are here!

• Possibility to receive CRA Certification!

• Exposure on international studies in different therapeutic areas

Desired Skills and Experience

• MUST! MSc degree with strong record of academic achievement, preferably in Scientific/Life Science field (Pharmacy, CTF, Biology, Chemistry etc.)

• MUST!2nd level Master in field of clinical research or previous experience as Study Coordinator or Data Manager

• Good understanding of clinical trial processes

• Proficiency both in English (written and spoken) and Italian

• Excellent Microsoft Office Skills

• Good communication skills

• Data accuracy

• Good interpersonal skills demonstrated as proactive, enthusiastic, and independent thinker

• Ability to be multi-tasking in a fast-paced environment and to work on a team

Location: IQVIA’s office – Milan

Internship grant

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.