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Training and Support

HSE Research and Development is committed to supporting the integration of research into policy and practice. Our goal is to foster a robust research culture in the health care sector and maximise the potential for positive impact.To support this mission, we offer a suite of training and support resources for researchers as well as for staff responsible for management and governance of research in the HSE or the HSE funded organisations. Training resources include guidance documents, HSeLanD courses and links to in webinars and training events

Below, you’ll find full details and an overview of all our available training resources and supports, designed to assist you in conducting high-quality research.

On this page, you’ll find:

Knowledge Translation and Dissemination Training and Resources

On this page you will find links to HSELand training and downloadable guides designed to help you plan your research so that it has the greatest possible impact on policy and practice.The resources introduce the principles of knowledge translation, outline how to plan for impact, and offer guidance on engaging stakeholders, choosing appropriate frameworks, evaluating your approach, and effectively communicating and disseminating research findings.

Resources include:

  • Seminars on Knowledge Translation
  • HSeLanD Knowledge Translation Modules
  • Guides and Resources on Knowledge Dissemination

Data Protection in Health and Social Care Research

On this page,  you will find practical guidance, templates, tools and recorded legal training to help researchers, and research managers apply data protection requirements to health and social care research. Resources cover topics including Data Protection Impact Assessments, retrospective chart reviews, pre-screening, consent, data controller and processor responsibilities, and international data transfers.

Resources include:

Practical Guidance on Data Protection for Health Researchers
Guidance on data protection requirements, HSE-tailored GDPR training and international data transfers.

Legal Insights in Health and Social Care Research
A 15-part webinar series developed with EY Law and CKT Solicitors, covering legal and data protection issues in research.

Templates and Tools Related to Research and Data Protection
Templates and supporting documents, including Data Protection Impact Assessments and Pre-Screening Agreements.

Research Integrity Training

These resources, accessible via HSELand, aim to help researchers understand best practices in responsible research behaviour and in line with the National Policy Statement on Ensuring Research Integrity in Ireland.

Public and Patient Involvement in Research

This page includes resources to help researchers understand the value and impact of PPI in research and how to incorporate PPI into their research projects. Resources include guidance on budgeting for PPI, identifying appropriate costs, applying good practice, understanding the role of PPI across the research process and knowledge translation, valuing PPI contributions and learning from examples of effective involvement.

Resources include:

  • Guides on Public and Patient Involvement in HSE Research
  • Useful Links and Resources for Public and Patient Involvement

Research Ethics

On this page, you’ll find information about Research Ethics Committees (RECs), which are a fundamental part of health research governance. RECs play a key role in protecting the safety, welfare, and rights of research participants. You’ll also find resources for researchers preparing to submit an ethics proposal, as well as guidance and supports for HSE and Hospital RECs.

Resources include:

  • Resources and Support for Applicants
  • Resources and Support for HSE and Hospital Research Ethics Committees
  • Training and Support for Patient and Public Contributors in RECs

National Electronic Research Management System

On this page, you will find training modules for researchers and research manager to support you in using the HSE National Electronic Research Management System (NERMS). NERMS is an online platform where researchers can apply for the approvals needed to conduct research in or with the HSE. 

Research Office Support

On this page, you’ll find information on the role of a Research Office and key supports for researchers and research managers. This includes guidance on the documentation that may be required, insurance and indemnity requirements, and resources for HSE and Hospital Research Offices such as research registration, legal agreements, and risk assessments. These resources are designed to make it easier to access clear guidance and to ensure research in the HSE is compliant, efficient, and impactful.