What are the responsibilities and job description for the Clinical Research Coordinator II position at HealthPartners?
We have an exciting opportunity for a Clinical Research Coordinator II to join our Critical Care Research Center! This position coordinates clinical trials within the Critical Care Research Center at Regions Hospital.
The Center oversees all research activities for the Emergency Medical Services program, the Emergency Department, the Burn Center, the Surgical Intensive Care Unit, and the Adult and Pediatric Level 1 Trauma programs. In partnership with the research project manager and director, this individual will assist in clinical trial design and implementation; oversee subject identification, recruitment and enrollment, data collection, and regulatory file management. This position will be responsible for initial IRB application and ongoing correspondence, including annual review reports. A primary job function for this individual is to develop and maintain effective working relationships with clinical staff, as well as applicable regulatory bodies. This individual may assist in data analysis, and manuscript preparation and submission as needed.
Work Schedule: Monday through Friday, 8 AM to 5 PM.
Required Qualifications:
- Bachelor’s degree in a healthcare, medical or science related field.
- Minimum of 3 years direct clinical research experience in a clinical, academic or industry setting.
Preferred Qualifications:
- Advanced graduate work in public health or comparable medical field.
- Experience in Biostatistics, research methodology.
- CCRC certification (SoCRA or ACRP) desired but not essential.
The Center oversees all research activities for the Emergency Medical Services program, the Emergency Department, the Burn Center, the Surgical Intensive Care Unit, and the Adult and Pediatric Level 1 Trauma programs. In partnership with the research project manager and director, this individual will assist in clinical trial design and implementation; oversee subject identification, recruitment and enrollment, data collection, and regulatory file management. This position will be responsible for initial IRB application and ongoing correspondence, including annual review reports. A primary job function for this individual is to develop and maintain effective working relationships with clinical staff, as well as applicable regulatory bodies. This individual may assist in data analysis, and manuscript preparation and submission as needed.
Work Schedule: Monday through Friday, 8 AM to 5 PM.
Required Qualifications:
- Bachelor’s degree in a healthcare, medical or science related field.
- Minimum of 3 years direct clinical research experience in a clinical, academic or industry setting.
Preferred Qualifications:
- Advanced graduate work in public health or comparable medical field.
- Experience in Biostatistics, research methodology.
- CCRC certification (SoCRA or ACRP) desired but not essential.
