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Clinical Research Data Management Specialist
2 weeks ago
About the Role
We are seeking a highly skilled and experienced Clinical Research Data Management Specialist to join our team at Beaumont Hospital. The successful candidate will be responsible for supporting the practice and development of research programmes within our institution, ensuring high-quality standards in all aspects of clinical research.
The ideal candidate will have a strong understanding of clinical research processes, excellent communication skills, and the ability to work independently as well as part of a team. They will also be familiar with electronic site files, research legislation, and regulatory frameworks.
Key Responsibilities
- Support the Programme Manager in maintaining high-quality standards in all aspects of clinical research.
- Assist with study start-up to ensure studies are opened in a timely manner.
- Oversee the introduction of an electronic site file across a broad portfolio of clinical research studies.
- Drive the move away from a paper-based environment with the adoption of electronic processes supported by internal and external means.
- Review monitoring visit letters and provide feedback to Principal Investigators and core team members on ways of improving data.
Required Skills and Qualifications
- A third-level qualification in healthcare/science/business or related area.
- A Master's or PhD degree in a relevant field such as science, nursing, or medicine.
- Experience working in Oncology/Haematology Clinical Trials units.
- Excellent understanding of clinical research processes.
- Familiarity with research legislation, regulatory frameworks, protocols, and ethics.