What are the responsibilities and job description for the Clinical Research Coordinator (Onsite) - Trauma Services position at CoxHealth?
Facility
CoxHealth South: 3801 S National Ave, Springfield, Missouri, United States of America, 65807
Department
1066 Trauma Program SGF
Scheduled Weekly Hours
40
Hours
08:00 am- 5:00 pm (Onsite)
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
***This position will work at Cox South Hospital, located in Springfield, Missouri***
The Trauma Clinical Research Coordinator is responsible for providing the overall administration and operation of clinical research trials involving the Trauma Service Line. This position requires knowledge of clinical protocols and good clinical practices, set forth by federal regulations and guidelines. Along with the investigators and the trauma services staff, this position is responsible, as directed by the Trauma Medical Director and the Trauma Program Manager 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 materials, e.g., survey and research charts, web-based materials, 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 Trauma Services Department. Must possess strong organizational skills and work in a self-directed team environment.
Education
▪ Required: Bachelor’s Degree in a clinical field such as biology, or closely related field;
▪ Preferred: Bachelor’s Degree in Nursing
Experience
▪ Preferred: Previous experience in pre-clinical or clinical research
Skills
▪ Working knowledge of Microsoft Word and Excel
▪ Good written and verbal communication
▪ Strong organizational skills
▪ Ability to multi-task and prioritize work at given time lines
Licensure/Certification/Registration
▪ Preferred: Certified as Clinical Research Coordinator and/or Clinical Research Associate
CoxHealth South: 3801 S National Ave, Springfield, Missouri, United States of America, 65807
Department
1066 Trauma Program SGF
Scheduled Weekly Hours
40
Hours
08:00 am- 5:00 pm (Onsite)
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 by Newsweek.
- Recognized as a Greatest Workplace for Women in both 2023 and 2024.
- Listed as one of the Greatest Workplaces for Diversity in 2024.
- Acknowledged by Forbes as one of the Best Employers for New Grads.
- Ranked among the Best Employers by State for Missouri.
- Healthcare Innovation's Top Companies to Work for in Healthcare in 2025.
- Medical, Vision, Dental, Retirement Plan with employer match, and many more!
- For a comprehensive list of benefits, please click here: Benefits | CoxHealth
***This position will work at Cox South Hospital, located in Springfield, Missouri***
The Trauma Clinical Research Coordinator is responsible for providing the overall administration and operation of clinical research trials involving the Trauma Service Line. This position requires knowledge of clinical protocols and good clinical practices, set forth by federal regulations and guidelines. Along with the investigators and the trauma services staff, this position is responsible, as directed by the Trauma Medical Director and the Trauma Program Manager 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 materials, e.g., survey and research charts, web-based materials, 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 Trauma Services Department. Must possess strong organizational skills and work in a self-directed team environment.
Education
▪ Required: Bachelor’s Degree in a clinical field such as biology, or closely related field;
▪ Preferred: Bachelor’s Degree in Nursing
Experience
▪ Preferred: Previous experience in pre-clinical or clinical research
Skills
▪ Working knowledge of Microsoft Word and Excel
▪ Good written and verbal communication
▪ Strong organizational skills
▪ Ability to multi-task and prioritize work at given time lines
Licensure/Certification/Registration
▪ Preferred: Certified as Clinical Research Coordinator and/or Clinical Research Associate