Union of http://terminology.hl7.org/CodeSystem/research-study-party-role and http://terminology.hl7.org/CodeSystem/research-study-party-role

This is the CodeSystem that contains all the codes in Research Study Party Role (http://terminology.hl7.org/CodeSystem/research-study-party-role) and Research Study Party Role (http://terminology.hl7.org/CodeSystem/research-study-party-role). E.g. what you have to deal with if you get resources containing codes in either of them

CodeSystem

Generated Narrative: CodeSystem 0dec4686-57e5-4818-b054-7867bc94809d-734

This code system http://hl7.org/fhir/comparison/CodeSystem/0dec4686-57e5-4818-b054-7867bc94809d-734 defines codes, but no codes are represented here

CodeDisplayDefinition
sponsor SponsorPerson, company, agency or institution that initiates a clinical investigation and takes responsibility for that investigation but does not conduct the investigation.
lead-sponsor Lead sponsorPrimary person, company, agency or institution that initiates a clinical investigation and takes responsibility for that investigation but does not conduct the investigation if there is more than one sponsor.
sponsor-investigator Sponsor-investigatorEntity who both initiates and conducts an investigation.
primary-investigator Principal investigatorAn investigator who is responsible for all aspects of the conduct of a study.
collaborator CollaboratorAn organization or individual, who contributes to a study by providing support to the primary investigator to conduct research.
funding-source Funding sourceAn organization that underwrites financial support for the research study.
general-contact General contactInformation for the person who can answer general questions for a study.
recruitment-contact Recruitment contactInformation for the person who can answer recruitment questions for a study.
sub-investigator Sub-investigatorAny individual member of the clinical trial team designated and supervised by the investigator at a trial site to perform critical trial-related procedures and/or to make important trial-related decisions (e.g., associates, residents, research fellows).
study-chair Study chairAn individual person who both initiates and conducts, alone or with others, a clinical trial and under whose immediate direction the investigational product is administered to, dispensed to, or used by a subject. (Also called study director or study chairperson)
irb Institutional Review BoardA group of individuals that reviews and monitors research involving human subjects.
data-monitoring Data MonitoringAn organization or individual who monitors the validity and integrity of collected data while prioritizing participant safety and study integrity. The organization may be called a Data Monitoring Committee (DMC) or Data and Safety Monitoring Board (DSMB).