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Clinical Research Associate

Grifols · Dublin, County Dublin, Ireland

Location
Dublin
Job Type
Regular Full-Time
Posted
June 07, 2026

Job Description

Assist in the clinical trial management to ensure timelines and metrics are met and maintained throughout the study. Provides support in the oversight and management of vendors. Conducts review of clinical data to ensure site adherence to applicable regulatory requirements, International Council on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) Good Clinical Practice (GCP) Guidelines, company standard operating procedures (SOPs), and study protocol.



What you'll do:

  • Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH GCP Guidelines, company SOPs, and study protocols. Ensure timelines and metrics are met and maintained throughout the study.

  • Has a good knowledge of the therapeutic area and product.

  • Obtains a complete understanding of all trial-related documents and operational procedures with moderate direc...

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