Clinical Research Coordinator II - Medical Oncology
Core
Assists investigators as a data coordinator for clinical research trials, extracting data from EMRs and entering it into EDC systems while ensuring protocol compliance and patient safety.
Role type
Clinical Research Coordinator
Builds
Clinical research trials and data integrity for medical oncology studies
Domain
Healthcare / Clinical Research
Required skills
Data extraction, Electronic Data Capture (EDC), Electronic Medical Record (EMR), Protocol management, Adverse event reporting, Regulatory compliance, Study design support, Data analysis, Manuscript preparation, Grant proposal support
Preferred skills
SOCRA/ACRP certification, Statistical Analysis Software (SAS), Spreadsheet Analysis
Technologies
EDC systems, EMR systems, SAS
Responsibilities
Extract data from EMRs and enter into EDC; ensure accurate collection of study-required procedures; manage and record data for all phases of study protocol; analyze and report adverse events; serve as liaison between the school, trial sponsors, vendors, and the study team; assist in developing research project plans and preparing manuscripts for publications.
Seniority
Mid-level, hands-on IC