Masters degree in Life Sciences, Project Management or related field and 3 years of experience involving the following Utilizing Electronic Data Capture EDC system or Clinical Trial Database such as iMedidata Rave or InForm, and evaluating EDC core configuration against study requirements; Ensuring Project deliverables and timelines are met by mitigating project risks and implementing and promoting the use of efficient quality control processes and standards within Data Management; Developing and maintaining Clinical Study Data Management documents such as Data Management Plan, eCRF electronic Case Report Form Instructions; Performing project levelbr coordination of daytoday oversight of all Data Management activities by executing the capture, cleaning, and storage of all clinical study data from initiation of study protocol through database lock; and Ensuring all Data Management activities are conducted in compliance with relevant global regulatory requirements for Clinical Research.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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