Clinical Research Coordinator - Hulston Cancer Center
About The Position
The Clinical Research Coordinator I is responsible for assisting in the overall administration and operation of clinical research trials at CoxHealth. This position requires a basic understanding of clinical protocols and good clinical practices, in accordance with federal regulations and guidelines. Working alongside investigators and research staff, the coordinator assists with daily activities such as collecting, maintaining, and organizing study information, files, materials, and equipment. Key tasks include scheduling and tracking patient visits, assisting with regulatory submissions, performing data entry, managing the timeliness of data submissions, preparing study-related materials (e.g., surveys, research charts, web-based instruments), updating and maintaining lists of study subjects, coordinating respondent mailings and interview logistics, and ensuring excellent documentation of research decisions and tasks. The role also involves performing any additional tasks necessary to support the Clinical Research department and its objectives.
Requirements
- Bachelor's Degree OR current Healthcare Credentials AND 2 years of experience
- Basic knowledge of clinical protocols and good clinical practices, as set forth by federal regulations and guidelines
- Strong organization skills
- Ability to multi-task and prioritize work to given time lines
- Good written and verbal communication
- Working knowledge of Microsoft Office software (Word, Excel, PowerPoint, Outlook)
Responsibilities
- Assist in providing the overall administration and operation of clinical research trials at CoxHealth
- Assist with the daily activities of collecting, maintaining and organizing study information, files, materials and equipment
- Schedule and track patient visits
- Assist with regulatory submissions
- Perform data entry and manage the timeliness of data submissions
- Prepare study related materials, e.g., survey and research charts, web-based instruments, etc.
- Update and maintain lists of study subjects
- Coordinate respondent mailings
- Coordinate interview logistics
- Maintain excellent documentation of research decisions and tasks
- Perform any additional tasks to support the Clinical Research department and its objectives, as needed
Benefits
- Medical
- Vision
- Dental
- Retirement with Employer Match
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
101-250 employees
