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IQVIA

Graduate Program Intern

Posted 16 Days Ago
Be an Early Applicant
2 Locations
Internship
2 Locations
Internship
The Graduate Program Intern will participate in a clinical research training program, working closely with supervisors and clinical staff to gain relevant experience in study procedures and project activities.
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Kickstart your career with IQVIA cFSP and engage in a bespoke graduate training and development program.

We are seeking graduates who are looking to develop a career in clinical research for a paid internship (9-month fixed term contract), with a view to become permanent (completion of the Graduate Program will not guarantee subsequent employment with the company).

Candidates must be based in Southwest England, Northeast England, Ireland or Northern Ireland.

The Internship is designed to offer a professional training program and requires the graduate to continuously demonstrate learning progress per training curriculum and supervisor feedback. Assignments will reflect the work being developed within the business department that are relevant for the graduate development and may include working as a member of a project team or independently in closely supervised projects/assignments.

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

*Please note - this role is not eligible for UK visa sponsorship*

Essential Functions

  • Participate and complete Graduate Program 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, monitoring support activities in accordance with contracted scope of work and good clinical practices. Assist CRA in updating tracking systems as needed.
  • Under close supervision, establishes 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 start-up phase.
  • Collaborate and liaise with study team members for project execution support as appropriate.
  • Under close supervision, perform other duties /learning activities as directed.

Qualifications

  • Bachelor’s degree (scientific discipline or health care) required.
  • Basic clinical research knowledge from courses or self-study preferred i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
  • Good written and verbal communication skills including good command of English language.
  • Good organizational and problem-solving skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

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

Top Skills

Excel
Microsoft Powerpoint
Microsoft Word

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