Clinical Research Coordinator

ID 2024-29570
Location
Cone Health Cancer Center
Work Location
US-NC-Greensboro
Division : Name
Cancer Center
Department : Name
WLCH-CHCC-Clinical Research
Category
PROFESSIONAL/MNGMNT
Position Sub-Category
CLINICAL
Position Type
Full Time (40 hours/week)
Employment Type
Employee
Exempt/NonExempt
Non-Exempt
FTE
1.00
Workforce Status
Onsite
Work Hours
40.00
Provider Schedule (specific schedule)
M-F. 830-1700
On call Required
No
Sub Category
Non-Clinical

Overview

 
The Clinical Research Coordinator works closely with study subjects and other research staff and is responsible for the day-to-day clinical research process to collect, compile, document, and analyze clinical research data. Working under direct supervision, the position assists the investigator with subject follow-up visits, completes clinical tasks, prepares research documentation, reports, and graphs while keeping appropriate logs, tracking participants, and preparing study materials. The schedule for this position is Monday - Friday, 8:30am - 5:00pm.

Talent Pool - Administrative & Clerica

Responsibilities

 

 
  • Coordinates multiple, less complex clinical trials simultaneously, managing and organizing various research activities efficiently, and ensuring optimal use of resources and timely execution of research protocols.
  • Serves as study coordinator for pharmaceutical and/or device trials, successfully coordinating site initiation visits, monitoring visits, and close-out visits, and ensuring adherence to protocol guidelines and regulatory requirements.
  • Completes clinical tasks (i.e., electrocardiogram (ECG), pulmonary function tests (PFT), phlebotomy, drug administration, etc.) when not prohibited by state or licensing board requirements under the supervision of the principal investigator.
  • Completes documentation in the electronic health/medical record (EMR) system to securely maintain patient health records.
  • Collects data from various sources, including patient charts, medical records, interviews, and diagnostic tests, and prepares comprehensive documentation, ensuring the accurate and reliable analysis of research data.
  • Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory compliance necessary for research projects in the hospital.
  • Assesses patients for protocol eligibility, ensuring the appropriate selection of participants for clinical trials, thereby enhancing the accuracy and validity of research outcomes.
  • Performs other duties as assigned.

Qualifications

 

EDUCATION:
Required: Bachelor's degree OR Associate's Degree (with 2 yrs experience) OR Healthcare/Health-related certification, e.g., EMT, Pharm Tech, Rad Tech, etc. (with 4 yrs experience)

 

EXPERIENCE:
Required: 4 Years (education and/or experience)

 

LICENSURE/CERTIFICATION/REGISTRY/LISTING:
Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification

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