Global Certificate in Clinical Trial Management: Trial Coordination

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The Global Certificate in Clinical Trial Management: Trial Coordination is a comprehensive course, designed to empower learners with the necessary skills to thrive in clinical research. This certificate course emphasizes the importance of trial coordination, a critical component in the conduction of clinical trials, ensuring data integrity, and compliance with regulatory standards.

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AboutThisCourse

In an industry where demand for skilled clinical trial professionals continues to rise, this course is instrumental in career advancement. Learners gain essential expertise in site management, regulatory affairs, informed consent, data management, and study close-out. The course also covers practical aspects like budgeting, project management, and vendor oversight. By the end of the course, learners are equipped with a broad understanding of clinical trial management, making them highly sought after in the global clinical research landscape. This course is not only beneficial for those seeking to excel in their current roles but also for those looking to transition into the clinical research industry.

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CourseDetails

• Trial Design and Protocol Development: Understanding the fundamentals of trial design, creating a protocol, and ensuring it meets regulatory requirements.
• Site Selection and Qualification: Identifying, assessing, and selecting suitable clinical trial sites and investigators.
• Budgeting and Contracting: Developing and managing budgets, contracts, and financial agreements with trial sites and vendors.
• Regulatory Affairs and Ethics: Navigating regulatory submissions, ethical approvals, and maintaining compliance throughout the trial.
• Project Management: Implementing project management strategies, tools, and best practices for successful trial coordination.
• Study Startup and Initiation: Executing site activation, training, and study initiation activities.
• Data Management: Overseeing data collection, data entry, data validation, and database management.
• Clinical Trial Monitoring: Coordinating on-site and remote monitoring activities to ensure data quality and patient safety.
• Quality Management and Quality Control: Implementing quality management systems and conducting quality control checks to ensure trial integrity.
• Clinical Trial Reporting and Closeout: Managing clinical study report preparation, statistical analysis, and closeout activities.

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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 £149
CompleteInOneMonth
AcceleratedLearningPath
  • ThreeFourHoursPerWeek
  • EarlyCertificateDelivery
  • OpenEnrollmentStartAnytime
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StandardMode GBP £99
CompleteInTwoMonths
FlexibleLearningPace
  • TwoThreeHoursPerWeek
  • RegularCertificateDelivery
  • OpenEnrollmentStartAnytime
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  • FullCourseAccess
  • DigitalCertificate
  • CourseMaterials
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GLOBAL CERTIFICATE IN CLINICAL TRIAL MANAGEMENT: TRIAL COORDINATION
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UK School of Management (UKSM)
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05 May 2025
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