
Set Up Specialist
- Dublin
- Permanent
- Full-time
- Coordinating the setup of clinical trials, including site selection, regulatory document preparation, and study material distribution.
- Collaborating with cross-functional teams to ensure alignment on study protocols, timelines, and operational requirements.
- Ensuring compliance with Good Clinical Practice (GCP) and other regulatory guidelines throughout the study setup phase.
- Providing ongoing support to study teams and sites, addressing any issues that arise during the trial setup process.
- Maintaining accurate records and documentation related to study setup activities.
- Bachelor’s degree in a relevant field such as life sciences, clinical research, or healthcare management.
- Experience in clinical trial setup, regulatory submissions, or site management, preferably within the pharmaceutical or biotechnology industry.
- Strong understanding of clinical trial processes, regulatory requirements, and GCP guidelines.
- Excellent organizational skills and attention to detail, with the ability to manage multiple setup tasks simultaneously.
- Strong communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.