Full-Time

Clinical Research Data Specialist 1

Posted on 10/31/2025

University of Southern California

University of Southern California

Compensation Overview

$26 - $34/hr

+

Los Angeles, CA, USA

In Person

Category
Biology & Biotech (7)
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Requirements
  • Minimum Education: Associate's degree, Combined experience/education as substitute for minimum education
  • Minimum Experience: 6 months
  • Minimum Field of Expertise: Requires good attention to detail with prior data entry experience. Some knowledge of medical terminology.
Responsibilities
  • Reads and understands clinical data from medical records. Extracts and enters required clinical data from medical records and patient research charts/reports to Clinical Research Forms (eCRFs/CRFs).
  • Maintains currency of research regulations including rules concerning reporting of Serious Adverse Events (SAEs) and violations with department training and feedback.
  • Interfaces with sponsors of externally sponsored trials. Provides timely data entry, plans and organizes monitoring visits and responds to inquiries.
  • Performs follow up for study patient survival by reviewing medical records. Contacts other institutions for data on patients hospitalized at other institutions.
  • Interacts closely with quality assurance teams to ensure data accuracy on Clinical Research Forms (eCRFs/CRFs) prior to submission for in-house, National Cancer Institute (NCI) sponsored and Cooperative Group studies. Discerns basic data discrepancies/protocol violations. Assists in obtaining outside documents and study specimen procurement and handling.
  • Attends new protocol start-up orientations. Completes required protocol specific training.
  • Assists in preparation of audits of assigned studies such as National Cancer Institute (NCI), Food and Drug Administration (FDA) and pharmaceutical audits.
  • Completes spreadsheets for industry studies in real time to ensure sponsor is invoiced appropriately and timely.
  • Ensures confidentiality, accuracy, security and appropriate access of all data and records.
  • Performs other related duties as assigned or requested. The university reserves the right to add or change duties at any time.
Desired Qualifications
  • Preferred Education: Associate’s Degree or combined experience/education as substitute for minimum education
  • Preferred Experience: Prior experience as a Data Manager in a clinical trials setting
  • Preferred Field of Expertise: Data Management
University of Southern California

University of Southern California

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