Preferred Label : Clinical Coordinator;
NCIt related terms : Clinical Research Coordinator (CRC); CLINICAL RESEARCH COORDINATOR; CRC; research coordinator; study coordinator; trial coordinator;
NCIt definition : A person to whom a clinical investigator delegates a few of the routine administrative
requirements of a protocol. The duties and responsibilities of a clinical research
coordinator may vary across different infrastructures. Generally, the coordinator
manages the subject's clinical trial participation and provides a vital linkage between
the subject, the investigator, and the sponsor.;
Alternative definition : CDISC: A qualified study staff member who manages the participation of subjects according
to the study protocol.; CDISC-GLOSS: A qualified study staff member who manages the participation of subjects
according to the study protocol. NOTE: CRCs coordinate communication among the subject,
investigator, and sponsor. Responsibilities may also include screening, enrollment,
monitoring of potential participants, and informed consent. [After Clinical Research
Manual: Practical Tools and Templates for Managing Clinical Research Cavalieri Jennifer
and Rupp Mark Clinical Research Manual: Practical Tools and Templates for Managing
Clinical Research 336pp US 44.95 Sigma Theta Tau 9781937554637 1937554635 [Formula:
see text]. Nurs Manag (Harrow). 2014 Aug 28;21(5):13.; After SOCRA]; MRCT-Ctr: A research staff member who helps manage studies. (https://mrctcenter.org/glossaryterm/clinical-research-coordinator-crc/);
Origin ID : C51811;
UMLS CUI : C4721857;
Automatic exact mappings (from CISMeF team)
- Semantic type(s)
- concept_is_in_subset
