Create a bespoke document in minutes, 聽or upload and review your own.
Get your first 2 documents free
Your data doesn't train Genie's AI
You keep IP ownership聽of your information
Research Service Agreement
"I need a Research Service Agreement for a Saudi pharmaceutical company engaging a US-based research institution to conduct clinical trials on a new diabetes medication, starting March 2025, with strict data protection and ethics compliance requirements."
1. Parties: Identification of the contracting parties, including full legal names, addresses, and registration details
2. Background: Context of the research services agreement and the parties' intentions
3. Definitions: Detailed definitions of key terms used throughout the agreement
4. Scope of Services: Detailed description of the research services to be provided
5. Term and Timeline: Duration of the agreement and key milestone dates
6. Payment Terms: Financial terms, including fees, payment schedule, and expenses
7. Intellectual Property Rights: Ownership and usage rights of research outputs, background IP, and foreground IP
8. Confidentiality: Protection of confidential information and trade secrets
9. Data Protection: Handling and protection of research data and personal information
10. Compliance with Laws: Obligation to comply with Saudi laws and relevant regulations
11. Representations and Warranties: Parties' assertions about their capacity and authority
12. Liability and Indemnification: Allocation of risks and responsibilities between parties
13. Force Majeure: Provisions for unforeseen circumstances preventing performance
14. Termination: Conditions and procedures for ending the agreement
15. Governing Law and Dispute Resolution: Application of Saudi law and dispute resolution mechanisms
1. Ethics and Compliance: Required for research involving human subjects or sensitive materials
2. Publication Rights: Include when academic or public dissemination of research results is contemplated
3. Export Control: Required for research involving controlled technologies or international collaboration
4. Background IP License: Include when existing intellectual property is being licensed for the research
5. Materials Transfer: Required when physical materials are being transferred for research
6. Third-Party Rights: Include when third-party materials or rights are involved in the research
7. Insurance: Required for high-risk research activities
8. Security Requirements: Include for sensitive research requiring specific security measures
1. Schedule 1 - Research Project Plan: Detailed description of research methodology, objectives, and deliverables
2. Schedule 2 - Payment Schedule: Detailed breakdown of payments, milestones, and payment conditions
3. Schedule 3 - Key Personnel: List of key researchers and their responsibilities
4. Schedule 4 - Background IP: Inventory of pre-existing intellectual property being contributed
5. Schedule 5 - Equipment and Facilities: List of research equipment and facilities to be used
6. Schedule 6 - Compliance Requirements: Specific regulatory and ethical requirements applicable to the research
7. Schedule 7 - Report Templates: Templates for progress reports and final deliverables
8. Appendix A - Data Management Plan: Protocols for data collection, storage, and sharing
Authors
Healthcare & Life Sciences
Technology & Innovation
Energy & Utilities
Manufacturing
Education
Environmental Sciences
Biotechnology
Petrochemicals
Agriculture
Aerospace & Defense
Financial Services
Mining & Minerals
Legal
Research & Development
Compliance
Intellectual Property
Finance
Operations
Innovation
Scientific Affairs
Technology Transfer
Contract Management
Risk Management
Quality Assurance
Research Director
Legal Counsel
Chief Scientific Officer
Research Project Manager
Compliance Officer
Intellectual Property Manager
Chief Technology Officer
Research and Development Manager
Contract Administrator
Head of Innovation
Chief Executive Officer
Research Scientist
Technology Transfer Officer
Research Operations Manager
Find the exact document you need
Research Cooperation Agreement
A Saudi Arabian law-governed agreement establishing terms for research collaboration between parties, including IP rights, resource sharing, and regulatory compliance.
Research Contract
A Saudi Arabian law-governed agreement establishing terms and conditions for research activities, including funding, IP rights, and compliance requirements.
Sponsored Research Agreement
A Saudi Arabian law-governed agreement establishing terms for sponsored research activities between funding entities and research institutions.
Research Service Agreement
Saudi Arabian law-governed agreement for research services, establishing terms for research conduct, intellectual property, and compliance requirements.
Data Use Agreement
A Saudi Arabian law-governed agreement establishing terms for data sharing and processing, ensuring compliance with PDPL and related regulations.
Confidentiality Agreement In Research
Saudi Arabian-governed confidentiality agreement for protecting sensitive research information and data, compliant with local research regulations and Islamic law.
Technology Transfer License Agreement
A Technology Transfer License Agreement under Saudi Arabian law, facilitating legal technology transfer between parties with local regulatory compliance.
Clinical Trial Contract
A Saudi Arabian law-governed agreement establishing the framework for conducting clinical trials, ensuring compliance with SFDA regulations and defining stakeholder responsibilities.
Confidential Disclosure Agreement In Clinical Research
A confidentiality agreement for clinical research activities in Saudi Arabia, ensuring SFDA compliance and protection of sensitive medical research information under Saudi law.
Market Research Agreement
A Saudi Arabian law-governed agreement outlining terms and conditions for market research services, including research methodology, deliverables, and compliance requirements.
Clinical Trial Confidentiality Agreement
A Saudi Arabian law-governed agreement protecting confidential information exchanged during clinical trials, ensuring compliance with SFDA regulations and Sharia law.
Clinical Study Agreement
A legal agreement for conducting clinical research studies in Saudi Arabia, governed by Saudi law and SFDA regulations, establishing terms between sponsors, institutions, and investigators.
Contract Research Agreement
A Saudi Arabian law-governed agreement establishing terms and conditions for collaborative research activities, including IP rights, financial terms, and research obligations.
Collaboration Research Agreement
A Saudi Arabian law-governed agreement establishing terms and conditions for collaborative research activities between multiple parties.
Download our whitepaper on the future of AI in Legal
骋别苍颈别鈥檚 Security Promise
Genie is the safest place to draft. Here鈥檚 how we prioritise your privacy and security.
Your documents are private:
We do not train on your data; 骋别苍颈别鈥檚 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 拢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.