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Salary
$24k – $46k per year (Estimated)
Location
In office (Istanbul)
Seniority
Intern
Employment
Full-Time

Confirmed on the employer's own hiring board on Sep 23, 2026. First seen by Alion on Sep 23, 2026. IQVIA scores B on the Alion truth index.

Overview
Company
Impact
Profile match
IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

We are looking for a highly motivated Graduate Program Clinical Research Trainee to join our Clinical Research team as part of a structured professional development program. This role is designed to provide hands-on training and practical experience in clinical research activities, allowing graduates to build their professional capabilities while working under close supervision in a regulated environment.

Key Responsibilities

  • Participate in and successfully complete the Graduate Program Clinical Research functional training curriculum, demonstrating satisfactory learning progress and performance.
  • Shadow experienced team members and learn clinical research functions and project-related activities under close supervision.
  • Complete required therapeutic area, protocol-specific, and clinical research training to support assigned responsibilities.
  • Engage in assignments specifically designed to build upon the academic background of the Graduate, with professional development as the primary focus of the role.
  • Demonstrate continuous learning and development in line with training curricula and regular supervisor feedback.
  • Work on assignments aligned with current business needs that support Graduate development, either as part of a project team or through closely supervised independent tasks.
  • Gain exposure to study procedures by working alongside experienced clinical staff.
  • Under close supervision, support monitoring-related activities in accordance with the contracted scope of work and Good Clinical Practice (GCP) guidelines.
  • Assist CRA/CTA teams by updating tracking systems and maintaining accurate study documentation as needed.
  • Establish regular communication with investigational sites, under guidance, to support ongoing project expectations and issue management.
  • Support assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment status, and data query resolution.
  • Provide support during the study start-up phase, as required.
  • Collaborate with study team members and cross-functional colleagues to support project execution.
  • Perform additional duties and learning activities as directed, under close supervision.

Qualifications

  • Recent graduate in Life Sciences, Health Sciences, or a related field.
  • Strong interest in pursuing a career in clinical research.
  • Ability to learn quickly and apply feedback in a structured training environment.
  • Good verbal and written communication skills in a professional setting.
  • Strong attention to detail, organizational skills, and willingness to work collaboratively.
  • Basic knowledge of clinical research principles is an advantage but not required.

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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