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Responsibilities of Clinical Investigation Assignment

   

Added on  2021-04-17

6 Pages1328 Words71 Views
Healthcare and Research
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RESPONSIBILITIES OF CLINICAL INVESTIGATORS 1RESPONSIBILITIES OF CLINICAL INVESTIGATORSBy CourseInstructorDate
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RESPONSIBILITIES OF CLINICAL INVESTIGATORS 2Introduction Clinical trials are investigations involving voluntary participation of people in the testing of new inventions and treatments that are aimed at managing, detecting and preventing different medical conditions and diseases. Clinical trials are carried out by clinical investigators who are referred to as medical researchers involved in clinical research. Clinical researchers are guided by fundamental principles and must meet specific responsibilities in the course of their investigation. This report will focus on various responsibilities of clinical research. Responsibilities of clinical researchers during clinical investigations range from protecting the welfare, safety, and rights of participants to observing professional codes guiding clinical research and adherence to the applicable regulations, investigational plan and investigators statement(1). By efficiently carrying out their responsibilities, clinical researchers help in protecting the integrity and values of their profession, and in enhancing the reliability of the outcome of clinical investigations.Maintaining Ethics in clinical research Ethics is a moral principle that guides individual’s behavior by defining what is wrong or right. Ethics is an important consideration not only in clinical research but also in other forms of research. It is the responsibility of clinical investigators to ensure that their clinical investigationsare carried out in an ethical manner (2). To achieve this they should be careful across all stages of clinical research. Decision on the trials to be carried out, carrying out actual investigation and conclusion of the clinical investigations are the main stages involved in clinical investigations and which call for the diligence of the clinical investigator. Although such investigations have
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RESPONSIBILITIES OF CLINICAL INVESTIGATORS 3regulatory safeguards, it is often the sole responsibility of the clinical investigator to ensure that research participants are treated equitably and fairly. In order to prevent any potential research issues, clinical investigators are tasked with the responsibility of thoroughly reviewing the research protocol .This will enable them to get an understanding of the study's primary endpoint and make it possible for them to identify any signs of deterioration of the investigation, which is likely to affect the outcome(3). Through promoting ethical research, clinical investigators ensurethat the wellbeing, safety, rights and dignity of research participants is prioritized at all times.Ensuring Informed participator consent Informed consent in clinical research refers to the voluntary agreement of an individual toparticipate in a clinical investigation. Apart from filling the consent form several other aspects about the research including its potential risks should be revealed to the participants before they can sign the consent form .It is the duty of the investigator to ensure that participants consent to their participation in a clinical study before being enrolled. It is the responsibility of the investigator to ensure that research participants are fully informed about the nature of the study before being enrolled (4). Participants should have all their questions sufficiently answered and be given an opportunity to decide on the interventions in which they wish to participate how theywant to be treated in the course of the study. The researcher should therefore at all times uphold the wishes and desires of research participants. In addition the researcher has the responsibility of informing research participants about the potential benefits and risks of participation in the research as well as any other alternative treatment options that they have. The research should also explain to the participants about the randomization and the fact that no one has the potential of determining the treatment arm to which different participants are assigned. This responsibility
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