AZ201-AstraZeneca Internship Program-Clinical Research Intern

As part of our AstraZeneca Internship Program, you’ll be involved in projects and learning opportunities that have real impact from day one. Being part of our journey and helping us to provide life changing medicine to patients all over the world and transform lives for the better. Making important contributions and embracing our values to deliver on our purpose. Because regardless of role or level, we all have an important part to play in making a positive difference.

Background & Qualifications

  • Being a 3rd / 4th year undergraduate student or a 1st year post graduate student in an accredited university
  • Able to work minimum 2,5 days availability per week
  • Good command of written and spoken English
  • Competent in MS Office applications (e.g. Word, Excel, PowerPoint)
  • Being able to accommodate in Istanbul during the intenship period
  • High degree of analytical thinking skills and the ability to analyze,
  • Having excellent communication skills
  • Customer and result-oriented.


Job Description

The Clinical Reserch Intern; assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. Typical Accountabilities are listed below;


  • Assists CSAs and CRAs for coordination and administration of clinical studies from the start-up to execution and close-out.
  • Collects, assists in preparation, reviews and tracks documents for the application process. Assists in timely submission of proper application/documents to EC/IRB and, where appropriate to Regulatory Authorities for the duration of the study.
  • Assists CSAs and CRAs during the document collection process to support effective delivery of a study and its documents.
  • Assist CSA and CRAs for maintenance of the eTMF & ISF.
  • Contributes to electronic applications/submissions by handling clinical-regulatory documents according to the requested technical standards i.e., Submission Ready Standards (SRS), supporting effective publishing and delivery to regulatory authorities
  • Contributes to the production and maintenance of study documents, ensuring template and version compliance.
  • Assist to CSAs for Preparation/support/perform Health Care Organizations (HCO)/Health Care Professionals (HCP) payments in accordance with local regulations.
  • Assist CSAs and CRAs to coordination and tracking of study materials and equipment


Where can I find out more?

  • Follow AstraZeneca on LinkedIn
  • Follow AstraZeneca on Instagram

For application please click.