Internship, Clinical Department

Contratto a tempo indeterminato
Non specificato

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Do you want to transform Clinical Development? 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?

Quintiles and IMS Health have come together to become IQVIA, The Human Data Science Company™ Inspired by the industry we help, IQVIA commits to providing solutions that enable life sciences companies to innovate with confidence, maximize their opportunities and ultimately drive human health outcomes forward.

We are currently looking for interns to join our Clinical teams in Milan.
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 manager and/or other designated clinical team members you will have the possibility to gain a complete overview of clinical roles such as CRA, Clinical Trial Assistant and Regulatory & Start Up.

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 and RSUs) in accurately updating and maintaining clinical systems that track site compliance and performance within project timelines
> Collaborate in the preparation site regulatory documents, reviewing for completeness and accuracy
> Be responsible for providing support to clinical projects under direction and supervision of line manager and/or other designated clinical team members

- Career & development opportunities - we are the leader CRO, opportunities are here!
- Exposure on international studies in different therapeutic areas

- MSc degree with strong record of academic achievement, preferably in Scientific/Life > Science field (Pharmacy, CTF, Biology, Chemistry etc.)
- 2nd level Master in field of clinical research will be considered a plus
- 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

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™.