INTERNSHIP DETAILS

Intern - Serbia

CompanyIQVIA
LocationBelgrade
Work ModeOn Site
PostedMay 22, 2026
Internship Information
Core Responsibilities
The intern will support clinical activities within the Site Management department through training and supervised tasks. The role focuses on learning Clinical Trial procedures and protocols, specifically regarding the Clinical Research Associate (CRA) role.
Internship Type
full time
Company Size
78251
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
About the Role

IQVIA Serbia is looking to engage an Intern to support our clinical activities in Site Management department. This entry-level role is designed for fresh graduates, or students close to graduation, with strong interest in Clinical Trials, Clinical Research Associate (CRA) or similar roles and career development within the CRO environment.

The role requires daily presence in our Belgrade office, with regular working hours.

Job overview:

  • The program is designed to educate Interns on Clinical Trial procedures and protocols within Site Management department, with emphasis on CRA and related roles.
  • The training is performed through series of online and on-site training courses, mentoring by our senior employees and by performing supervised tasks within the scope of work. The training can also include introduction to other departments and supervised on-site monitoring visits.
  • When the Internship is successfully finished, the Intern should have a good overview of the world of Clinical Trials and be ready for his/her/their next career step.
  • The duration of the internship is set to 6 months. During this period, successful candidate will be contractually engaged through youth cooperative.

Qualifications:

  • Bachelor's degree (or close to graduation), MD or Pharmacist preferred.
  • Fluency in Serbian and English language.
  • Good communication skills and strong motivation to pursue a career in Clinical trials environment.
  • General understanding and interest in Pharma industry, Clinical research, CRO companies and CRA role.
  • Driver´s license (in place or upcoming).

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.

Key Skills
Clinical TrialsClinical ResearchSite ManagementCommunication SkillsEnglish FluencySerbian FluencyPharma Industry Knowledge
Categories
HealthcareScience & ResearchConsulting