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The Certified Research Administrator (CRA) is a designation granted in the United States by the Research Administrators Certification Council to individuals who demonstrate the knowledge necessary to serve as an administrator of professional and sponsored research programs. [1]
A clinical research associate (CRA), also called a clinical monitor or trial monitor, is a health-care professional who performs many activities related to medical research, particularly clinical trials. Clinical research associates work in various settings, such as pharmaceutical companies, medical research institutes and government agencies.
The National Council of University Research Administrators (NCURA) was initiated in 1958 to aid in the evolution of the profession of Research Administration from that of a part-time job performed by persons with other primary duties into that of a full-time profession with specific requirements.
Obtaining a certificate is voluntary in some fields, but in others, certification from a government-accredited agency may be legally required to perform certain jobs or tasks. Organizations in the United States involved in setting standards for certification include the American National Standards Institute (ANSI) and the Institute for ...
A Clinical Research Coordinator (CRC) is a person responsible for conducting clinical trials using good clinical practice [1] (GCP) under the auspices of a Principal Investigator (PI). Good clinical practices principles have been defined by Madelene Ottosen, RN, MSN, of The University of Texas Health Science Center at Houston [ 2 ] as:
Certified Risk Analyst (CRA) is a risk management professional designation offered by the Global Academy of Finance and Management (GAFM). CRA risk management training and certification is available in New York , California , Asia , the Middle East and other locations.
The Certified IRB Professional (CIP) program is a certification initiative in the United States for individuals administering and overseeing the daily activities of institutional review boards (IRBs). IRBs are committees that are charged with determining if a research project conforms to ethical principles and federal regulations that protect ...
Certified Research Administrator; Clinical research associate or Clinical Research Assistant in clinical trial; Commander, Royal Artillery; ... Corona Australis (CrA