Position Details
About this role
RDC I is responsible for the data management of multiple research projects and extracting data from medical records to populate study databases; works with the study coordinator and monitors to ensure data is captured per protocol.
Key Responsibilities
- Review and synthesize medical records data to extract trial data
- Ensure data capture per study protocol
- Consult with study coordinator and sponsors on data requirements
- Report data into study database systems
- Resolve data queries and support data capture
Technical Overview
Supports data collection and reporting for clinical trials; uses study database systems and follows regulatory guidelines; hybrid work arrangement.
Ideal Candidate
The ideal candidate is an entry-level clinical research data coordinator with 1 year of data processing or data management experience, capable of reviewing medical records and extracting trial data, and following regulatory guidelines to populate study databases.
Must-Have Skills
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
No High School Diploma or GED and no AA/AS degree, Lack of experience with automated data processing techniques, Unwillingness to work hybrid in Tampa
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