Clinical Trial Process

Level 2

  • 1

    Module 1: Site Selection for a Trial

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    • Knowledge Checkpoints 01

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  • 2

    Module 2: Trial Start-up Requirements: From Site Selection to Site Initiation

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  • 3

    Module 3: Trial Active Stage: Managing the Subjects and Monitoring

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    • Knowledge Checkpoints 01

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    • Knowledge Checkpoints 02

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  • 4

    Module 4: After patient completion: Responsibilities for the data, the documents and reporting results

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    Module 5: Trial Master File and Site Files – Design, Management and Archiving

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    • Knowledge Checkpoints 1

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    • Knowledge Checkpoints 2

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    • Knowledge Checkpoints 3

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Instructor

Chief Operating Officer

Dr Tina Barton

Dr. Tina Barton, Chief Operating Officer of eMQT, is a drug development specialist with over 40 years’ experience, working in partnership to lead for success as a customer-focused senior leader. During this time Dr. Barton has invested in training for the future – through team leadership, individual mentoring and training thereby sharing knowledge and developing professionals. Through her role at the Institute of Clinical Research she continues to support and lead training activities. With a passion for transformation, Dr. Barton drove the embracement of Central Eastern European countries and now is focused on the inclusion of Sub-Saharan Africa into clinical development – bringing the miracle of development of new medicines to emerging markets and new patients. Dr. Barton holds a BSc, PhD and MBA alongside over 50 academic publications and is an Honorary Fellow, and Board Member of the Institute of Clinical Research.