Get Northeastern University Assurance of Principal Investigator 2017-2024

Investigators play a crucial role in protecting the rights and welfare of human subjects and are responsible for carrying out sound ethical research consistent with research plans approved by an IRB.

Principal investigators (PI) are responsible for obtaining Institutional Review Board (IRB) approval before beginning any human subjects research. When you submit a protocol to the IRB for review as the PI, you agree to comply with federal regulations and University policies and procedures for the study duration.

Investigators play a crucial role in protecting the rights and welfare of human subjects and are responsible for carrying out sound ethical research consistent with research plans approved by an IRB.

Background: Institutional review boards (IRBs), duly constituted under the Office of Human Research Protection, have the federally mandated responsibility of reviewing research involving human subjects to ensure that a proposed protocol meets the appropriate ethical guidelines before subjects may be enrolled in any ...

Principal investigators (PI) are responsible for obtaining Institutional Review Board (IRB) approval before beginning any human subjects research. When you submit a protocol to the IRB for review as the PI, you agree to comply with federal regulations and University policies and procedures for the study duration.

Background: Institutional review boards (IRBs), duly constituted under the Office of Human Research Protection, have the federally mandated responsibility of reviewing research involving human subjects to ensure that a proposed protocol meets the appropriate ethical guidelines before subjects may be enrolled in any ...

Principal Investigator (PI) – A Principal Investigator is the primary individual responsible for the preparation, conduct, and administration of a research grant, cooperative agreement, training or public service project, contract, or other sponsored project in compliance with applicable laws and regulations and ...

Principal Investigator (PI) – A Principal Investigator is the primary individual responsible for the preparation, conduct, and administration of a research grant, cooperative agreement, training or public service project, contract, or other sponsored project in compliance with applicable laws and regulations and ...

Researchers need to ensure that participants understand the risks and benefits if they choose to participate in the study, as well as implementing appropriate designs and data management practices that will respect participants' rights.

Researchers need to ensure that participants understand the risks and benefits if they choose to participate in the study, as well as implementing appropriate designs and data management practices that will respect participants' rights.

The individual responsible for the conduct of a clinical study at a site is the principal investigator (PI). While there are many advantages to being a PI for a clinical trial, PIs are subject to numerous restrictions designed to ensure patient safety and meaningful study results.

The Principal Investigator is responsible for the management and integrity of the design, conduct, and reporting of the research project and for managing, monitoring, and ensuring the integrity of any collaborative relationships.

IRBs represent the federal government and the local agencies involved in reviewing research and are responsible for protecting the rights and welfare of research participants at a particular institution.

The individual responsible for the conduct of a clinical study at a site is the principal investigator (PI). While there are many advantages to being a PI for a clinical trial, PIs are subject to numerous restrictions designed to ensure patient safety and meaningful study results.

Human Subjects Rights All activities involving humans as research participants must provide for the safety, health, and welfare of every individual. Rights, including the right to privacy, must not be infringed. No participant in a research activity shall be exposed to unreasonable risk to health or well-being.

The Principal Investigator is responsible for the management and integrity of the design, conduct, and reporting of the research project and for managing, monitoring, and ensuring the integrity of any collaborative relationships.

The Principal Investigator (PI) is ultimately responsible for assuring compliance with applicable University IRB policies and procedures, DHHS Federal Policy Regulations, and FDA regulations and for the oversight of the research study and the informed consent process.

IRBs represent the federal government and the local agencies involved in reviewing research and are responsible for protecting the rights and welfare of research participants at a particular institution.

Principal investigator (PI) refers to the person(s) in charge of a clinical trial or a scientific research grant. The principal investigator prepares and carries out the clinical trial protocol (plan for the study) or research paid for by the grant.

Human Subjects Rights All activities involving humans as research participants must provide for the safety, health, and welfare of every individual. Rights, including the right to privacy, must not be infringed. No participant in a research activity shall be exposed to unreasonable risk to health or well-being.

The Principal Investigator (PI) is ultimately responsible for assuring compliance with applicable University IRB policies and procedures, DHHS Federal Policy Regulations, and FDA regulations and for the oversight of the research study and the informed consent process.

Principal investigator (PI) refers to the person(s) in charge of a clinical trial or a scientific research grant. The principal investigator prepares and carries out the clinical trial protocol (plan for the study) or research paid for by the grant.