Clinical Research Data Specialist I
Core
Extracts and enters clinical data from medical records and patient charts into Clinical Research Forms (eCRFs/CRFs) for in-house, NCI, and Cooperative Group studies.
Role type
Clinical Research Data Specialist I
Builds
Clinical Research Forms (eCRFs/CRFs) for National Cancer Institute (NCI) and Cooperative Group studies
Domain
Healthcare / Clinical Trials
Required skills
Data entry, Attention to detail, Medical terminology knowledge, Data accuracy verification, Protocol violation identification, Audit preparation
Preferred skills
None stated
Technologies
eCRFs/CRFs, Spreadsheets
Responsibilities
Reads and understands clinical data from medical records; Maintains currency of research regulations including SAE reporting; Interfaces with sponsors of externally sponsored trials; Performs follow up for study patient survival by reviewing medical records; Interacts with quality assurance teams to ensure data accuracy; Assists in preparation of audits for NCI, FDA, and pharmaceutical audits; Completes spreadsheets for industry studies.
Seniority
Entry-level (6 months experience)