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Confidentiality Agreement For Research Participants
"I need a Confidentiality Agreement for Research Participants for a medical research study in Jakarta involving collection of sensitive health data and genetic information, starting in March 2025, with potential data sharing with international research partners."
1. Parties: Identifies the research institution/researcher and the research participant
2. Background: Explains the context of the research project and the need for confidentiality
3. Definitions: Defines key terms including 'Confidential Information', 'Research Project', 'Personal Data', and other relevant terms
4. Purpose of Agreement: States the specific purpose for which confidential information will be shared and used
5. Scope of Confidential Information: Clearly defines what information is considered confidential within the research context
6. Participant Obligations: Details the participant's responsibilities regarding confidentiality and data protection
7. Researcher Obligations: Outlines how the research team will protect and handle the participant's information
8. Data Protection and Privacy: Specifies measures for protecting personal data in compliance with Indonesian law
9. Duration of Confidentiality: Specifies how long the confidentiality obligations remain in effect
10. Return or Destruction of Information: Procedures for handling confidential information after research completion
11. Permitted Disclosures: Circumstances under which confidential information may be disclosed
12. Breach and Remedies: Consequences of breaching the agreement and available remedies
13. Governing Law and Jurisdiction: Specifies Indonesian law as governing law and relevant jurisdiction
14. Execution: Signature block and execution details
1. Publication Rights: Include when research results may be published, specifying how participant confidentiality will be maintained
2. Third Party Disclosure: Include when other researchers or institutions may need access to the confidential information
3. Digital Data Handling: Include when research involves electronic data collection and storage
4. Recording and Photography: Include when research involves audio/visual recording of participants
5. Withdrawal Rights: Include when participants have the right to withdraw from the research
6. Cultural Sensitivity: Include when research involves culturally sensitive information or indigenous knowledge
7. Medical Information Handling: Include when research involves collection of medical or health data
1. Research Project Description: Detailed description of the research project, methodology, and types of information to be collected
2. Data Protection Protocols: Specific procedures and safeguards for protecting confidential information
3. Consent Form: Separate research consent form that works in conjunction with this agreement
4. Information Sheet: Detailed information about the research project and participant involvement
5. Contact Information: List of key contact persons including researchers, supervisors, and ethics committee representatives
Authors
Academic Research
Medical Research
Social Sciences
Psychology
Market Research
Clinical Trials
Pharmaceutical Research
Public Health
Educational Research
Anthropological Studies
Consumer Research
Technology Research
Environmental Studies
Behavioral Sciences
Legal
Research & Development
Ethics & Compliance
Data Protection
Academic Affairs
Clinical Operations
Research Administration
Regulatory Affairs
Human Subject Protection
Research Ethics
Research Director
Principal Investigator
Research Ethics Officer
Research Coordinator
Data Protection Officer
Legal Counsel
Research Administrator
Ethics Committee Member
Research Compliance Manager
Academic Researcher
Clinical Research Manager
Research Project Manager
Human Subjects Protection Specialist
Research Ethics Administrator
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