![]() Submit invoice payment requests and maintaining payment tracker.Support Institutional Review Board (IRB) submissions including initial submissions, continuing reviews, and study close out reports.Track subject enrollment and study status across multiple active studies.Draft and complete interim monitoring visit reports and follow up letters.Reviewing the case report form (CRF) against the subject's medical record or source documentation for completeness and accuracy.Verification of the informed consent form (ICF) for each study subject.Performing monitoring activities at study site as able with training as applicable. ![]() Tracking and processing of study photographs, devices and equipment.Assist in drafting study data deliverables including clinical study reports,.Data management including obtaining, reviewing, and filing study data, data entry, source data verification, query generation, quality check and data cleaning, and data analysis.Ensure the completion, filing and maintenance of the required study regulatory documents and study data electronically for multiple studies.Skills required include photocopying, scanning, printing of labels and compiling the study related materials ![]()
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