Create a bespoke document in minutes, Â or upload and review your own.
Get your first 2 documents free
Your data doesn't train Genie's AI
You keep IP ownership of your information
Sponsored Research Agreement
"I need a Sponsored Research Agreement under Swiss law for a pharmaceutical company funding a 3-year clinical research project at a Swiss university, with specific provisions for human subject research and data protection, starting March 2025."
1. Parties: Identification of the sponsor and research institution, including full legal names and addresses
2. Background: Context of the research project, parties' expertise, and reasons for collaboration
3. Definitions: Key terms used throughout the agreement
4. Research Project: Detailed description of research scope, objectives, and methodology
5. Principal Investigator: Designation and responsibilities of the lead researcher
6. Performance Period: Timeline, milestones, and duration of the research project
7. Financial Terms: Budget, payment schedule, and financial obligations
8. Intellectual Property Rights: Ownership and rights to research results, background IP, and foreground IP
9. Confidentiality: Protection and handling of confidential information
10. Publications: Rights and procedures for publishing research results
11. Representations and Warranties: Parties' assurances regarding capacity, authority, and compliance
12. Liability and Indemnification: Allocation of risks and responsibilities
13. Term and Termination: Duration, renewal, and termination conditions
14. Governing Law and Jurisdiction: Swiss law application and dispute resolution procedures
15. General Provisions: Standard clauses including notices, amendments, and assignment
1. Human Subjects Research: Required when research involves human participants, including ethical compliance and informed consent
2. Equipment and Materials: Include when sponsor provides specific equipment or materials for research
3. Multi-Party Provisions: Required when multiple research institutions or collaborators are involved
4. Background Technology License: Include when existing technology is being licensed for use in the research
5. Commercialization Rights: Include when there are specific terms for commercial exploitation of research results
6. Data Protection: Required when research involves processing personal data
7. Export Control: Include when research involves internationally controlled materials or technology
8. Student Involvement: Required when students will participate in the research
9. Force Majeure: Optional clause for unforeseeable circumstances affecting research performance
1. Schedule A - Research Plan: Detailed description of research methodology, objectives, and deliverables
2. Schedule B - Budget: Detailed breakdown of costs, payment schedules, and financial arrangements
3. Schedule C - Timeline: Project timeline with milestones and deliverable dates
4. Schedule D - Personnel: List of key researchers and their responsibilities
5. Schedule E - Background IP: Inventory of relevant pre-existing intellectual property
6. Schedule F - Reporting Requirements: Format and frequency of progress reports and deliverables
7. Appendix 1 - Ethics Approvals: Copies of relevant ethical clearances and approvals
8. Appendix 2 - Material Transfer Terms: Specific terms for transfer and use of research materials
9. Appendix 3 - Data Management Plan: Procedures for data collection, storage, and sharing
Authors
Life Sciences
Pharmaceuticals
Biotechnology
Information Technology
Engineering
Healthcare
Environmental Sciences
Materials Science
Energy
Agricultural Science
Medical Devices
Chemical Industry
Artificial Intelligence
Robotics
Clean Technology
Legal
Research & Development
Business Development
Academic Affairs
Technology Transfer
Intellectual Property
Finance
Compliance
Scientific Affairs
Contracts Administration
Innovation
Grants Management
Research Director
Legal Counsel
Chief Scientific Officer
Principal Investigator
Research Manager
Contracts Manager
Technology Transfer Officer
Head of R&D
Chief Technology Officer
Research Administrator
IP Manager
Grant Manager
Business Development Director
Scientific Project Manager
Compliance Officer
Academic Affairs Director
Innovation Manager
Research Partnership Manager
General Counsel
Finance Director
Find the exact document you need
Clinical Research Contract
Swiss-law governed agreement for conducting clinical research studies, establishing terms between research institutions, sponsors, and investigators.
Academic Collaboration Agreement
Swiss law-governed agreement establishing terms for academic research collaboration between institutions.
Research Contract
A Swiss law-governed agreement establishing terms and conditions for research activities, including intellectual property rights, confidentiality, and research parameters.
Sponsored Research Agreement
Swiss law-governed agreement establishing terms for sponsored research collaboration between a funding entity and research institution.
Research License Agreement
A Swiss law-governed agreement establishing terms for licensed use of intellectual property or technology in research activities.
Data Use Agreement
Swiss-law governed agreement establishing terms for data sharing and usage between parties, incorporating FADP/nFADP requirements.
Studentship Agreement
A Swiss law-governed agreement between an educational institution and student establishing the terms of enrollment and study program obligations.
Investigator Agreement
Swiss law-governed agreement defining terms and conditions for conducting clinical trials by investigators, ensuring compliance with Swiss regulations and ICH-GCP guidelines.
Confidentiality Agreement For Research Participants
A Swiss-law governed confidentiality agreement for research participants, ensuring data protection and confidentiality in research studies while complying with Swiss regulations.
Confidentiality Agreement In Research
A Swiss law-governed Confidentiality Agreement for protecting sensitive information in research projects, compliant with federal and cantonal requirements.
Biobank Agreement
Swiss law-governed agreement for managing biological sample collection, storage, and usage in biobank facilities, ensuring regulatory compliance and ethical operations.
Data Transfer Agreement Clinical Trial
Swiss-law governed Data Transfer Agreement for clinical trials, ensuring compliant transfer and protection of trial data under Swiss regulations.
Clinical Research Agreement
Swiss-law governed agreement for conducting clinical research studies, establishing terms between research institutions, sponsors, and investigators under Swiss regulatory framework.
Accelerated Clinical Trial Agreement
Swiss-law governed agreement for conducting accelerated clinical trials, establishing expedited processes while ensuring regulatory compliance and patient safety.
Indirect Cost Agreement
A Swiss law-governed agreement establishing the framework for calculating and allocating indirect costs between business entities, including methodology, reporting, and audit requirements.
Research Grant Agreement
A Swiss law-governed agreement establishing terms and conditions for research funding between a grant-giving institution and recipient, including funding terms, research obligations, and compliance requirements.
Clinical Trial Confidentiality Agreement
Swiss law-compliant confidentiality agreement for protecting sensitive information in clinical trials, aligned with Swiss data protection regulations and international research standards.
Letter Of Intent For Research Collaboration
A Swiss-law governed preliminary document outlining the framework and intentions for a research collaboration between parties, serving as a foundation for a detailed future agreement.
Contract Research Agreement
A Swiss law-governed agreement establishing terms for commissioned research activities, including IP rights, confidentiality, and delivery requirements.
Download our whitepaper on the future of AI in Legal
³Ò±ð²Ô¾±±ð’s Security Promise
Genie is the safest place to draft. Here’s how we prioritise your privacy and security.
Your documents are private:
We do not train on your data; ³Ò±ð²Ô¾±±ð’s AI improves independently
All data stored on Genie is private to your organisation
Your documents are protected:
Your documents are protected by ultra-secure 256-bit encryption
Our bank-grade security infrastructure undergoes regular external audits
We are ISO27001 certified, so your data is secure
Organizational security
You retain IP ownership of your documents
You have full control over your data and who gets to see it
Innovation in privacy:
Genie partnered with the Computational Privacy Department at Imperial College London
Together, we ran a £1 million research project on privacy and anonymity in legal contracts
Want to know more?
Visit our for more details and real-time security updates.
Read our Privacy Policy.