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Intern - Graduate Programme

On-site in Reading·Full-time·Added 7 days ago (last checked 8 Oct)

IQVIA

264 open roles

Overview

Job details

  • Full-time

    Per the ad.

Requirements

  • Work on-site in Reading

    No relocation package mentioned.

Skills

Nice to have

Requirements

What we're looking for

  • Bachelor's or Master's degree in scientific or healthcare discipline required.

Nice to have

  • Basic clinical research knowledge obtained through coursework or self‑study preferred (e.g., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines).

Pay & benefits

Visa & relocation

Please note: this role is not eligible for UK visa sponsorship.

The role

Kickstart your career with IQVIA cFSP and engage in a bespoke graduate training and development programme.

We are seeking graduates who are looking to develop a career in clinical research for a paid internship (9‑month fixed-term contract), with the potential to become permanent. (Please note: completion of the Graduate Programme does not guarantee subsequent employment with the company.)

The internship is designed to offer a professional training programme and requires graduates to demonstrate continuous learning progress in line with the training curriculum and supervisor feedback. Assignments will reflect work undertaken within the business department and may include contributing to project teams or working independently on closely supervised tasks.

Apply today to forge a career with greater purpose, make an impact, and never stop learning!

What you'll do

  • Participate in and complete the Graduate Programme CRA training curriculum.
  • Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
  • Shadow and learn functions and/or project activities under close supervision.
  • Gain experience in study procedures by working with experienced clinical staff.
  • Under close supervision, support monitoring activities in accordance with the contracted scope of work and Good Clinical Practice. Assist CRAs with updating tracking systems as required.
  • Under close supervision, establish regular lines of communication with sites to help manage ongoing project expectations and issues.
  • Under close supervision, provide support to assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, and data query resolution. May also support the start‑up phase.
  • Collaborate and liaise with study team members to support project execution as appropriate.
  • Under close supervision, perform other duties and learning activities as directed.

What We're Looking For

  • Computer skills, including proficiency in Microsoft Word, Excel and PowerPoint.
  • Ability to establish and maintain effective working relationships with colleagues, managers and clients.

Hiring process

1 interview

  • Other interviews are conducted on Microsoft Teams, unless otherwise specified.
  • Most interviews are conducted in English unless otherwise specified. However, some questions may be asked in local language.
  • The use of AI support during an interview or online assessment is strictly prohibited and grounds for disqualification.

About IQVIA

Industry
Clinical Research and Health Data
Founded
1982
Employees
50,000–100,000
Headquarters
Durham, USA
Website
iqvia.com

In their own words

About the company & team

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 https://jobs.iqvia.com

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.

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