Intern

About Us

IQVIAis the largest provider of biopharmaceutical development and commercial outsourcing services and a global leader in healthcare intelligence. With a global team of 67000 working across 100 countries we harness insights commercial and scientific depth and executional expertise to empower clients to achieve some of their most important goals: Improving clinical scientific and commercial results. Realizing the full potential of innovations and ultimately building solutions for our clients to drive healthcare forward.

A career withIQVIA connects you to great opportunity to achieve professional success and impact healthcare around the world. At IQVIA youll have training and development to plan and progress your career in the direction you choose; we do not believe in a career ceiling.

We are currently offering a 9 months full - time (37h pw) Internship.

Start date 1st June 2023!

During the internship you will have the possibility to deepen your knowledge of the clinical research 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.

Essential Functions
Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors studies as well as reconcile the total GPS Sponsor balance to the Corporate Sponsor Balance on a monthly basis per SSAE16 Controls
Responsible to accurately complete all necessary journal entries as assign
Responsible to quality review CTA and Payment Intake form setups to determine appropriate SAP vendor and payment method for Payments staff for assigned Sponsors studies inclusive of bank entry validation for the Accounting dept.
Responsible for SharePoint tracker completion for assigned sponsors.
On an annual basis assist with 1099 and other country tax reporting as assigned
Special projects involving maintenance of the vendor database in SAP and SOP Maintenance as required
Other duties as assigned

Qualifications
Bachelors Degree
Appropriate verbal and written communication skills to function within a professional work environment.
Evidence of effective problem solving analytical and critical thinking skills.
Proficiency in alignment with the desired role placement
Evidence of strong team work and communication skills.

During your internship you will have the possibility to:

• Be trained on clinical research world and IQVIAs 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 IQVIAs 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

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.