IQVIA

Summer Internship Program in Clinical Trials

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.

IQVIA Summer Internship program provides interns with:

Insight into the most important phases of a clinical trial;
Experience working alongside Clinical Research Associates;
Exposure to working in a challenging, international business environment;
The opportunity to see whether a career in Clinical Research is right for you;

We are looking for a talented & highly motivated undergraduate or fresh graduate to gain first-hand experience in the field of Clinical Research. During the internship you will become a valuable member of our clinical team by contributing to individual projects aimed to develop your career.

The ideal candidate is a last year student or graduate at Medical/Scientific University with excellent communication skills in local language and in English. Personally you demonstrate enthusiasm to grow and to develop further in the Clinical Research area.

Internship program terms & conditions:

Duration: 2 months (July-August)
Full-time official employment
Intern are eligible for salary

Clinical Trials Assistant

Join us on our exciting journey!

At IQVIA, we know that meaningful results require not only the right approach but also the right people. Regardless of your role, you’ll have the opportunity to play an important part in helping our clients improve patient healthcare. You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information & technology areas, you can seek opportunities to change and grow without boundaries.

Do you want to contribute to the improvement of the global healthcare? Are you looking for a starting point in clinical research? This is why Clinical Trials Assistant role is here for you.

WHAT WOULD BE YOUR ROLE:

Act as a central contact for the team for assigned project communications, correspondence and associated documentation.
Assist colleagues with accurately updating and maintaining systems that track site compliance and performance within project timelines.
Support the preparation, handling, distribution, filing, and archiving of clinical documentation and reports.
You may accompany Clinical Research Associates on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.

WHAT SKILLS & KNOWLEDGE IS IMPORTANT TO HAVE:

Background: High or Secondary School diploma/certificate or country’s educational equivalent in Life Science will help you to deal with specific language of clinical trials and medical terminology. We appreciate awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
English language: fluent English is essential for communication within international environment at IQVIA.
PC skills: You should be able to work with Microsoft Word, Excel and PowerPoint and quickly get familiar with specialised software of IQVIA.
Working experience: previous experience in clinical trials area or general administrative role will be an asset.
Planning & multitasking: We will assign you with several projects at a time. Therefore, you will have a lot of urgent tasks to do.
Attention to detail & accuracy: behind each document is a real patient. You should keep a sharp eye on every detail of the document to ensure compliance with all procedures and regulations.
Collaboration: we do expect you to establish and maintain effective working relationships with coworkers, managers and clients.

Equivalent combination of education, training and experience would be also sufficient for the role.

WHAT WE HAVE TO OFFER:

We put special emphasis in offering the best training opportunities and fostering personal development. Our culture is based in improving the well-being of our employees, both at professional and personal levels. We offer flexibility, recognition and rewards as well as an attractive salary

Clinical Research Associate / Senior Clinical Research Associate

Join us on our exciting journey!

Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

Award winning and innovative, we’ll give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You’ll be building a smart and flexible career with no limits.

While projects vary, your typical responsibilities might include:

Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Supporting the development of a subject recruitment plan
Establishing regular lines of communication plus administering protocol and related study training to assigned sites
Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

You should have:

A Bachelor's degree in a health care or other scientific discipline or educational equivalent
At least 1 year of on-site monitoring experience
Alternatively, you should have an equivalent combination of education, training and experience

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™.