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Clinical Research Associate – Multi‑Sponsored Model

iqvia · Belgrade

New
🇬🇧 English

Job description

About the role

Join a leading global CRO as a Clinical Research Associate working on multi‑sponsored studies. You will support site selection, initiation, monitoring and close‑out while ensuring high‑quality data collection.

Key responsibilities

  • Perform site selection, initiation, monitoring and close‑out visits and maintain appropriate documentation.
  • Support the development of subject recruitment plans and track recruitment progress.
  • Establish regular communication with sites and deliver protocol and study training.
  • Evaluate site practices for quality and integrity, escalating issues when necessary.
  • Manage study progress by tracking regulatory submissions, case report form completion and data query resolution.

Required profile

  • Bachelor’s degree in a health‑care related field (MD or Pharmacist preferred).
  • At least 1 year of on‑site monitoring experience.
  • Fluent written and verbal English and Serbian.
  • Valid driver’s licence for frequent travel to sites.

Questions fréquentes

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Source : ats:workday

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Published 9 hours ago

Expires 1 month from now

3 views · 0 interested

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iqvia

Belgrade