
Senior Research Coordinator
4 days ago
This is a home-based role with occasional travel to our office. You will be working exclusively on Irish studies, requiring independent work and task ownership.
Key Responsibilities:- Communicate with project teams and track study activities for Irish trials
- Maintain essential documentation and ensure regulatory compliance
- Support site and study material preparation
- Assist with meeting coordination, minute-taking, and documentation
- Manage Trial Master File (TMF) documentation and quality control
- Liaise with vendors and coordinate study supply shipments
- Provide general administrative and systems support
Requirements:
- Minimum of 12 months' experience in Clinical Research Administration (CRO or Pharma)
- Experience supporting clinical trials in Ireland is preferred
- Strong ability to work independently and manage time effectively
- Basic understanding of biology and clinical trial processes
- Excellent organizational and communication skills
The Perfect Opportunity:
You'll develop your skills in a supportive environment, working on complex, high-quality clinical trials in Ireland. This role offers flexibility while giving you the chance to make a real impact.
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