Certificate in Trial Participant Screening

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The Certificate in Trial Participant Screening is a crucial course for those interested in clinical research and healthcare industries. This program highlights the importance of identifying, screening, and selecting eligible candidates for clinical trials, ensuring high-quality research data and ethical conduct.

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AboutThisCourse

With the growing demand for clinical trials and the increasing focus on personalized medicine, the importance of proper trial participant screening cannot be overstated. Learners will gain essential skills in study design, regulatory compliance, and communication, enhancing their career opportunities in various healthcare settings. Upon completion, students will be equipped with the knowledge and competencies necessary to effectively contribute to clinical research teams, leading to improved patient outcomes and advancements in medical treatments. Stand out in the competitive healthcare industry by mastering the art of trial participant screening.

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• Eligibility Criteria: Understanding the basic requirements for trial participation including medical history, age, and lifestyle factors.

• Screening Process: Outlining the steps involved in the trial participant screening process, from initial contact to final selection.

• Informed Consent: Explaining the importance of informed consent in clinical trials and the process of obtaining it from potential participants.

• Confidentiality and Data Protection: Ensuring the confidentiality and protection of participant data during the screening process and throughout the trial.

• Exclusion Criteria: Identifying the factors that may exclude a potential participant from a clinical trial, such as existing medical conditions or medications.

• Pre-Trial Assessments: Describing the assessments and tests conducted prior to trial participation to ensure participant safety and trial validity.

• Trial Design and Objectives: Familiarizing participants with the design and objectives of the clinical trial, including the study drug or intervention and expected outcomes.

• Clinical Trial Phases: Explaining the different phases of clinical trials and their significance in the development of new treatments.

• Risks and Benefits: Balancing the potential risks and benefits of trial participation, including the possibility of receiving placebo or standard of care treatment.

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EntryRequirements

  • BasicUnderstandingSubject
  • ProficiencyEnglish
  • ComputerInternetAccess
  • BasicComputerSkills
  • DedicationCompleteCourse

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  • NotAccreditedRecognized
  • NotRegulatedAuthorized
  • ComplementaryFormalQualifications

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CourseFee

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FastTrack GBP £140
CompleteInOneMonth
AcceleratedLearningPath
  • ThreeFourHoursPerWeek
  • EarlyCertificateDelivery
  • OpenEnrollmentStartAnytime
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StandardMode GBP £90
CompleteInTwoMonths
FlexibleLearningPace
  • TwoThreeHoursPerWeek
  • RegularCertificateDelivery
  • OpenEnrollmentStartAnytime
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  • FullCourseAccess
  • DigitalCertificate
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CERTIFICATE IN TRIAL PARTICIPANT SCREENING
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London College of Foreign Trade (LCFT)
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05 May 2025
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