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Sponsored Research Agreement
"I need a Sponsored Research Agreement for a three-year pharmaceutical research project starting January 2025, where a Dublin-based biotech company is funding research at Trinity College Dublin, with specific requirements for handling clinical trial data and potential commercialization rights."
1. Parties: Identification of the sponsor and research institution, including full legal names and addresses
2. Background: Context of the research project, relationship between parties, and general objectives
3. Definitions: Defined terms used throughout the agreement, including technical and project-specific terminology
4. Scope of Research: Detailed description of research objectives, methodologies, and deliverables
5. Duration and Timelines: Project duration, key milestones, and any extension provisions
6. Financial Provisions: Payment terms, research funding, payment schedule, and eligible costs
7. Intellectual Property Rights: Ownership and licensing of background and foreground IP, publication rights
8. Confidentiality: Protection of confidential information, duration of obligations, and permitted disclosures
9. Project Management: Governance structure, key personnel, reporting requirements, and meeting schedules
10. Warranties and Indemnities: Standard warranties, limitations of liability, and indemnification provisions
11. Data Protection: GDPR compliance, data handling procedures, and data security measures
12. Termination: Termination rights, procedures, and consequences
13. General Provisions: Standard boilerplate clauses including governing law, notices, and entire agreement
1. Human Subjects Research: Required when research involves human participants, including ethics committee approvals and consent procedures
2. Material Transfer: When physical materials are being transferred between parties for research purposes
3. Equipment Usage: When significant research equipment is provided by either party
4. International Collaboration: Required for cross-border research, including export control compliance
5. Student Involvement: When students are involved in research, including thesis rights and academic requirements
6. Background IP License: Detailed licensing terms when significant background IP is being licensed for the research
7. Commercialization Rights: When there's potential for commercial exploitation of research results
8. Publication Review Process: Detailed procedures for reviewing and approving academic publications
9. Third Party Rights: When other parties have rights in the research or its outputs
1. Schedule 1 - Research Plan: Detailed technical description of research methodology, objectives, and deliverables
2. Schedule 2 - Budget and Payment Schedule: Detailed breakdown of costs and payment milestones
3. Schedule 3 - Key Personnel: List of key researchers and their roles/responsibilities
4. Schedule 4 - Background IP: Inventory of relevant background IP brought to the project
5. Schedule 5 - Equipment and Materials: List of key equipment and materials to be used/provided
6. Schedule 6 - Reporting Requirements: Templates and schedules for project reports
7. Schedule 7 - Data Management Plan: Detailed procedures for data collection, storage, and sharing
8. Appendix A - Template Forms: Standard forms for various procedures (e.g., publication approval, material transfer)
9. Appendix B - Insurance Requirements: Specific insurance coverage requirements for both parties
Authors
Agreement
Background Intellectual Property
Background Materials
Commencement Date
Confidential Information
Data Protection Laws
Deliverables
Effective Date
Field of Research
Force Majeure Event
Foreground Intellectual Property
Good Research Practice
Grant
Improvements
Intellectual Property Rights
Key Personnel
Know-How
Materials
Milestones
Personal Data
Principal Investigator
Project
Project Manager
Project Plan
Project Results
Research
Research Location
Research Period
Research Program
Research Reports
Research Team
Sponsor
Sponsored Research
Student
Technical Information
Term
Third Party
Work Product
Grant of Rights
Research Scope
Project Management
Financial Terms
Payment
Intellectual Property Rights
Background IP
Foreground IP
Publication Rights
Confidentiality
Data Protection
Research Standards
Regulatory Compliance
Ethics Approval
Research Materials
Equipment Use
Key Personnel
Student Involvement
Reports and Deliverables
Record Keeping
Warranties
Indemnification
Limitation of Liability
Insurance
Force Majeure
Term and Termination
Consequences of Termination
Assignment
Dispute Resolution
Governing Law
Notices
Entire Agreement
Severability
Variation
Waiver
Third Party Rights
Survival
Interpretation
Pharmaceuticals
Biotechnology
Information Technology
Medical Devices
Healthcare
Environmental Sciences
Agricultural Science
Clean Energy
Manufacturing
Materials Science
Artificial Intelligence
Telecommunications
Food Science
Chemical Engineering
Space Technology
Legal
Research and Development
Innovation
Intellectual Property
Academic Affairs
Contracts Administration
Research Operations
Technology Transfer
Compliance
Scientific Affairs
Grant Management
Commercial Operations
Research Director
Legal Counsel
Chief Scientific Officer
Research Program Manager
Head of R&D
Technology Transfer Officer
Intellectual Property Manager
Research Grant Administrator
Commercial Director
Chief Technology Officer
Research Compliance Officer
Contract Manager
Innovation Director
Academic Affairs Director
Research Ethics Officer
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