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:
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Submit ApplicationJob Details
- Location Dublin, County Dublin
- Job Type Regular Full-Time
- Category Life, Physical, and Social Science Technicians
- Posted Date July 05, 2026
- Application Deadline August 14, 2026