Clinical Research Coordinator - Hulston Cancer Center

Facility:

Hulston Cancer Center: 3850 S National Ave, Springfield, Missouri, United States of America, 65807

Department:

1375 Cancer Research for the Ozarks

Scheduled Weekly Hours:

40

Hours:

8:00 AM - 5:00 PM

Work Shift:

Day Shift (United States of America)

CoxHealth is a leading healthcare system serving 25 counties across southwest Missouri and northern Arkansas. The organization includes six hospitals, 5 ERs, and over 80 clinics. CoxHealth has earned the following honors for workplace excellence:

 

• Named one of Modern Healthcare’s Best Places to work five times.

• Named one of America’s Greatest Workplaces, Greatest Workplaces in Healthcare (2025, 2026), Greatest Workplaces for Women (2023, 2024), and Greatest Workplaces for Diversity (2024) by Newsweek and Plant-A Insights Group. 

• Acknowledged by Forbes as one of the Best Employers for New Grads.

• Healthcare Innovation's Top Companies to Work for in Healthcare (2025).

 

Benefits

• Medical, Vision, Dental, Retirement with Employer Match and more (20+ hrs/week)  

• For a comprehensive list of benefits, please click here: Benefits | CoxHealth

Job Description:

Job Profile Summary
The responsibility of the Clinical Research Coordinator I is to assist in providing the overall administration and operation of clinical research trials at CoxHealth. This position requires basic knowledge of clinical protocols and good clinical practices, as set forth by federal regulations and guidelines. Along with the investigators and the research staff, this position is responsible, as determined by the Director of Clinical Research, for assisting with the daily activities of collecting, maintaining and organizing study information, files, materials and equipment; scheduling and tracking patient visits; assisting with regulatory submissions; performing data entry and managing the timeliness of data submissions; preparing study related materials, e.g., survey and research charts, web-based instruments, etc.; updating and maintaining lists of study subjects; respondent mailings; coordinating interview logistics; and maintaining excellent documentation of research decisions and tasks; any additional tasks to support the Clinical Research department and its objectives, as needed.

Education:
Required: Bachelor's Degree OR 8 years of relevant healthcare/research experience
Experience:
No experience required
Skills:
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)
Licensure/Certification/Registration:
N/A