Clinical Research Coordinator - Lublin

Are you looking for an opportunity to work with an industry‑leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Lublin.

This role with an immediate start is for 24 hours per week and is expected to last around 11 months . This is an onsite role in Lublin.

The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.

Responsibilities

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including :

• Maintaining up‑to‑date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
• Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.)
• Planning and coordinating logistical activity for study procedures according to the study protocol
• Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
• Management and shipment of biological samples
• Coordinating with study monitor on study issues and effectively responding to monitor‑initiated questions
• Administrative research task

Qualifications

If this sounds like the perfect opportunity for you, please apply now!

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

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