GENERAL SUMMARY/ OVERVIEW STATEMENT:
The Cancer Center Protocol Office is seeking motivated, detail-oriented individuals to join our team as a Clinical Research Data Specialist (CRDS). The Cancer Center Protocol Office is a centralized research office that supports clinical researchers in all disciplines within the Cancer Center. Our office promotes and facilitates clinical research by providing comprehensive services to physicians conducting clinical trials while ensuring compliance with all regulatory requirements.
The CRDS works independently under minimal supervision to extract clinical data and research data from electronic medical records and other sources and enter into electronic data capture system utilized for the clinical research protocol. The CRDS will be responsible for entering data for multiple oncology clinical trials. This position is fully remote.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
The CRDS will perform the following responsibilities independently under minimal supervision by the Clinical Research Manager:
SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:
EDUCATION:
EXPERIENCE:
SUPERVISORY RESPONSIBILITY:
WORKING CONDITIONS: