A health care professional responsible for the conduct of a clinical study at a study site. If a team of individuals at a study site conducts a study, the investigator is the responsible leader of the team and may be called the principal investigator.
The contractor's employee who is primarily responsible for conducting the study.
A researcher responsible for conducting a clinical trial at a trial site.
a scientist who devotes himself to doing research
a medical professional, usually a physician, under whose direction an investigational drug is administered to a human volunteer
an interactive, step-by-step multimedia training course that provides effective instruction on how to conduct both design and process FMEAs
A researcher in a treatment study. Often, this is an Oncologist.
CDC staff who are working directly or in collaboration with an outside party in the design of a research study, development of methods and procedures for the study, collection of data, analysis of data, or interpretation of data; a coauthor.
The principal investigator, co-investigator and other OHSU employees or volunteers, or any OHSU research collaborator, including visiting scientists, responsible for the design, conduct or reporting of research or educational activities or responsible for preparing a proposal for research funding. "Investigator" includes the Investigator's spouse and dependent children.
A research doctor or dentist who does the Clinical Trial.
A health professional involved in the design, conduct, analysis, or interpretation of the clinical trial, generally including doctors, nurses, pharmacists, and coordinators.
A scientist or engineer who is a member of the research and development team, either on the laboratory staff or the staff of a contractor, and who plays a key role (other than as a consultant) in a given project.
A medical professional, usually a physician, under whose direction an investigational drug is administered or dispensed. A principal investigator is responsible for the overall conduct of the clinical trial at his/her site.
a clinical researcher who is involved with a clinical trial protocol and its implementation. The Principal Investigator is ultimately responsible for the conduct of the trial.
A study physician who oversees the running of a clinical trial at a particular site is referred to as an investigator. If multiple physicians become involved at a single site, the first physician to participate is typically considered the principal investigator and the others, sub-investigators.
A person responsible for the conduct of the clinical trial at a trial site. If a trial is conducted by a team of individuals at a trial site, the investigator is the responsible leader of the team and may be called the principal investigator.
Physicians involved in clinical trials are referred to as investigators, since they are investigating the safety of, and efficacy of new medical products.
An investigator is the experienced clinical researcher who prepares a protocol or treatment plan and implements it with patients.
The person in charge of carrying out a clinical study. May also be referred to as "principal investigator."
An individual who attends and participates in a research project.
In clinical trials, an individual who actually conducts an investigation [21 CFR 312.3]. Any interventions (e.g., drugs) involved in the study are administered to subjects under the immediate direction of the Investigator.
A researcher in a clinical trial or clinical study.
Often, a lawsuit will require more extensive investigation. An experienced law firm can properly provide a private investigator for collection of additional evidence, such as witness statements, photographs of an accident site, or background research and/or location of potential defendants.