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Administrative roles or clinical trial administrators who support the day to day activities for the trial
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Field-based monitors or clinical research associates who travel to different research units to ensure the trial is running correctly
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Clinical study/project managers who manage the teams or running of the trial (usually on a region or global level)
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Directorship roles where the person will have the sole responsibility for a trial
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Our Teams have a lot of interaction with people in a range of other departments including clinical science, clinical quality assurance, data management, biostatistics and regulatory affairs to ensure that the data and information needed by these other departments is delivered so they can decide if a trial has been successful
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Development of protocol and other study documents
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Identification of clinical trial sites and investigators
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Training, startup, and management of clinical sites
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Managing logistics of study materials.
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Providing a channel of communication between research teams specializing in clinical science, statistics, pharmacovigilance, data science, regulatory activities, legal, and marketing, while keeping them up to date and on task.
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Fiscal management
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Identifying project risks and planning for changes ahead of time
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Internal and external stakeholder management.
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Quality management
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Trial closeout and reporting