IQVIA

Intern in Site Management department - Serbia

Serbia · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

  • EmployerIQVIA
  • LocationSerbia
  • Work styleWork style not stated
  • Employment typeFull time
  • Employer posted

IQVIA Serbia is looking to hire an Intern to support our clinical activities.
Position is full time, with 6 months fix term contract, office based in Belgrade.

The program is designed to educate Interns on Clinical Trial procedures and protocols within Site Management department, with emphasis on Clinical Research Associate (CRA) role, but will also cover Clinical Site Activation (CSA) roles and responsibilities.
The training is performed through online and in office training, mentoring by our seniors employees and by performing supervised tasks within the scope of work.

When the Internship is successfully finished, the Intern should have a good overview of the world of Clinical Trials, CRA and CSA job responsibilities and be ready for their next career step.

Qualifications:

  • Bachelor’s degree in Life Sciences required; degrees in Pharmacy and Medicine (MD) are preferred.
  • Fluency in Serbian and English language is a must
  • Good communication skills and strong motivation to pursue a career in clinical trials environment
  • General knowledge on and interest in pharma industry, Clinical Research and CRO companies
  • Available to work as office based, full time, Mon-Fri
Show full description

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.

Staying safe while you apply

  • Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
  • Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
  • Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

  • Check the fit.

    Compare the requirements with the experience you have confirmed, including gaps.

  • Prepare honestly.

    Build interview stories and application drafts from your own evidence.

  • Keep track.

    Save the role and record your own application status and follow-ups.

Create a free workspace or log in.

At a glance

  • Employment typeFull time
  • SeniorityIntern
  • Employer posted
  • Added to ROLIVA
  • Last checked

Explore similar roles

Similar jobs