What are the responsibilities and job description for the Clinical Information Specialist position at Technical Resources International, Inc.?
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.
- 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.