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Investigator Agreement

Investigator Agreement Template for New Zealand

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Key Requirements PROMPT example:

Investigator Agreement

"I need an Investigator Agreement under New Zealand law for a multi-site pharmaceutical trial starting March 2025, with special emphasis on data protection and cross-border data sharing provisions as we'll be collaborating with Australian research centers."

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Document background
The Investigator Agreement serves as a crucial legal document in New Zealand's research landscape, establishing the framework for conducting clinical trials and research studies. It is essential when engaging qualified professionals to conduct research activities, whether in clinical, academic, or commercial settings. The agreement ensures compliance with New Zealand's regulatory requirements, including the Health and Disability Commissioner Act 1994, Privacy Act 2020, and Health Research Council guidelines. It covers critical aspects such as study protocol adherence, participant safety, data protection, intellectual property rights, and reporting obligations. This document is particularly important for maintaining regulatory compliance, protecting all parties' interests, and ensuring research integrity within New Zealand's jurisdiction.
Suggested Sections

1. Parties: Identifies the contracting parties - typically the research institution/sponsor and the investigator

2. Background: Explains the context of the research study and the purpose of the agreement

3. Definitions: Defines key terms used throughout the agreement

4. Appointment and Scope: Establishes the investigator's appointment and outlines the scope of their responsibilities

5. Study Protocol: References and incorporates the study protocol and requires compliance with it

6. Regulatory Compliance: Requires compliance with applicable laws, regulations, and ethical guidelines

7. Investigator Obligations: Details specific duties and responsibilities of the investigator

8. Institution/Sponsor Obligations: Outlines the obligations of the institution/sponsor

9. Confidentiality: Addresses confidentiality obligations regarding study data and information

10. Data Protection: Specifies requirements for handling personal and research data

11. Intellectual Property: Addresses ownership and rights to research results and innovations

12. Payment Terms: Specifies compensation and payment arrangements

13. Term and Termination: Defines the duration and termination provisions

14. General Provisions: Includes standard legal provisions such as governing law, dispute resolution, and assignment

Optional Sections

1. Sub-Investigators: Include when the investigator will be working with sub-investigators who need to be covered by the agreement

2. Equipment and Supplies: Include when specific equipment or supplies will be provided for the study

3. Publication Rights: Include when addressing rights to publish study results

4. Insurance: Include when specific insurance requirements need to be detailed

5. Conflict Resolution: Include when specific dispute resolution procedures are required beyond general provisions

6. Study Budget: Include when detailed financial arrangements need to be incorporated into the main agreement

Suggested Schedules

1. Study Protocol: Detailed protocol for the research study

2. Payment Schedule: Detailed breakdown of payment terms and milestones

3. Timeline: Study timeline and key milestones

4. Required Documentation: List of required documentation and reports

5. Data Management Plan: Detailed procedures for data collection, storage, and handling

6. Ethical Guidelines: Relevant ethical guidelines and requirements

7. Insurance Certificates: Copies of required insurance certificates

8. CV and Qualifications: Investigator's curriculum vitae and relevant qualifications

Authors

Alex Denne

Head of Growth (Open Source Law) @ ¶¶Òõ¶ÌÊÓƵ | 3 x UCL-Certified in Contract Law & Drafting | 4+ Years Managing 1M+ Legal Documents | Serial Founder & Legal AI Author

alex.den.21@genieai.co
Relevant legal definitions
















































Clauses






























Relevant Industries

Healthcare

Pharmaceuticals

Biotechnology

Medical Devices

Clinical Research

Academic Research

Public Health

Life Sciences

Healthcare Technology

Medical Education

Relevant Teams

Legal

Clinical Operations

Research and Development

Medical Affairs

Regulatory Affairs

Clinical Development

Research Administration

Compliance

Ethics Committee

Data Management

Quality Assurance

Contract Management

Research Governance

Relevant Roles

Principal Investigator

Clinical Research Director

Research Coordinator

Medical Director

Clinical Trial Manager

Research Scientist

Chief Medical Officer

Academic Researcher

Clinical Operations Manager

Research Program Director

Study Site Manager

Medical Science Liaison

Research Compliance Officer

Clinical Development Director

Industries









Teams

Employer, Employee, Start Date, Job Title, Department, Location, Probationary Period, Notice Period, Salary, Overtime, Vacation Pay, Statutory Holidays, Benefits, Bonus, Expenses, Working Hours, Rest Breaks,  Leaves of Absence, Confidentiality, Intellectual Property, Non-Solicitation, Non-Competition, Code of Conduct, Termination,  Severance Pay, Governing Law, Entire Agreemen

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