Masters degree in Life Science, Clinical Research Administration, or related field 6 years of experience involving the following Overseeing the quality and scientific integrity of clinicalbr operations for studies; Monitoring the execution of the clinical study against timelines, deliverables, and budget; Planning and managing the clinical study execution in accordance with abr global program strategy; Providing input into and lead the development of studyspecific plans including case report forms, data management plans, and monitoring plans; Managingbr identification, selection, setup, or management of vendors; and Communicating study status including timelines and deliverables to stakeholders such as clinical study team, programbr managers, therapeutic area heads, or global development leads.br br Section H.14 defines the experience and skills that a qualified candidate must possess to meet the actual minimum requirements for the position. This experience and skills may be obtained in the position offered or any alternate related occupation, regardless of job title.
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