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Research Grant Agreement
"I need a Research Grant Agreement under Irish law for a €500,000 medical research project between Trinity College Dublin and a pharmaceutical company, with specific provisions for clinical trials and commercialization of research outcomes."
1. Parties: Identification of the grant-giving organization and the recipient institution/researcher
2. Background: Context of the research grant, including the application process and selection
3. Definitions: Definitions of key terms used throughout the agreement
4. Grant Award: Details of the grant amount, payment schedule, and eligible costs
5. Research Project: Description of the approved research project, objectives, and methodology
6. Duration: Term of the grant agreement and any extension provisions
7. Obligations of the Recipient: Key responsibilities of the grant recipient, including research conduct and reporting
8. Financial Management: Requirements for managing grant funds, maintaining records, and financial reporting
9. Intellectual Property Rights: Ownership and management of IP created during the research
10. Publication and Dissemination: Rights and obligations regarding the publication of research results
11. Monitoring and Reporting: Requirements for progress reports and project monitoring
12. Confidentiality: Protection of confidential information shared during the project
13. Termination: Conditions and process for early termination of the grant
14. General Provisions: Standard legal clauses including governing law, notices, and amendment procedures
1. Equipment and Assets: Include when the grant covers purchase of significant equipment or assets
2. Clinical Trial Provisions: Required for research involving clinical trials or human subjects
3. Data Protection: Detailed section required when research involves personal data processing
4. International Collaboration: Include when research involves international partners or cross-border activities
5. Student Involvement: Include when postgraduate students will be involved in the research
6. Commercialization: Include when research has potential commercial applications
7. Background IP License: Include when existing IP will be used in the research
8. Ethics and Research Governance: Detailed section required for sensitive research areas
1. Schedule 1 - Research Project Description: Detailed description of the research project, methodology, and timeline
2. Schedule 2 - Budget and Payment Schedule: Detailed breakdown of the grant budget and payment milestones
3. Schedule 3 - Key Personnel: List of principal investigators and key researchers involved
4. Schedule 4 - Reporting Requirements: Detailed reporting templates and schedules
5. Schedule 5 - Equipment List: Inventory of equipment to be purchased or used
6. Appendix A - Research Ethics Approval: Copies of relevant ethics committee approvals
7. Appendix B - Data Management Plan: Details of data collection, storage, and sharing procedures
8. Appendix C - Publication Protocol: Procedures for publishing and disseminating research results
Authors
Higher Education
Scientific Research
Biotechnology
Medical Research
Technology Innovation
Environmental Science
Agricultural Research
Engineering
Social Sciences
Humanities
Pharmaceutical Research
Clean Energy
Digital Technology
Marine Science
Healthcare
Legal
Research Administration
Finance
Compliance
Technology Transfer Office
Research Development
Contracts
Academic Affairs
Research Ethics
Project Management
Grants Office
Intellectual Property
Research Operations
Risk Management
Academic Governance
Research Director
Principal Investigator
Grant Administrator
Legal Counsel
Research Officer
Finance Manager
Compliance Officer
Technology Transfer Officer
Research Development Manager
Contract Manager
Department Head
University Registrar
Research Ethics Officer
Project Manager
Academic Supervisor
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