Clinical Information Specialist

Job Description Abstracts protocol and/or contact/site/organization information into the appropriate databases for use by the client and their collaborators in support of clinical trials.Maintains data quality for protocol specific data and mastered level record.Responds to phone or email queries regarding standard processes associated with the abstractions.Uploads protocols and protocol-related documents to the appropriate Document Library and manages uploaded documents.Assists in the preparation of contract required reports.Takes notes at meetings and provides a summary of the meeting minutes to the client.Disseminates study information to required collaborators.Stays current on relevant legislation and announcements regarding research.Participates in the revision/creation of SOPs, work instructions, and task specific manuals as necessary and appropriate.Handles special client requests as assigned.Works closely with offices both internal and external to ensure that data is properly conveyed and analyzed.Other duties as assigned. Job Requirements Scientific or medical background preferred.Excellent oral, written, interpersonal, and organizational skills.Solid computer skills including Microsoft Office. This is a hybrid position with 2 days in TRI's Bethesda, Maryland office, and 3 days working remotely.