Job Listing
|
|
| Job ID: 13834342 |
|
| |
| Job Location: |
|
| |
|
|
| |
| How to Apply: | To see employer contact information, log in or register. |
| |
| Job Title: | Clinical Research Coordinator |
| Work Type: | Work Days: Weekdays, Work Vary: No , Shift: First (Day), Hours Per Week: 40, Work Type: Regular |
| |
| Salary Offered: | Unspecified |
| Benefits: | 401(k) or other retirement, Dental Insurance, Health Insurance, Holidays, Sick Leave or PTO, Vacation or PTO, Vision Plan |
| |
| Physical Required: | Unspecified |
| Drug Testing Required: | Unspecified |
| Education Required: | High School Diploma/GED |
| |
| Experience Required: | 36 Months |
| |
| Required Skills: | See job description |
| Preferred Skills: |
|
| |
| |
| |
|
| Job Description: |
MN Urology is seeking a Full Time Clinical Research Coordinator
Minnesota Urology is the largest independent urologic specialty practice in the state of Minnesota and was formed as an integration of Minnesota's two most respected independent urology practices; Minnesota Urology and Urology Associates. Our providers are devoted to a singular vision to deliver optimal and compassionate specialty care. Our success and recognition as a national leader in the practice of urology is a direct result of the collective work of dedicated staff members and physicians.
Primary Objective
The Clinical Research Coordinator (CRC) is responsible for the coordination of clinical research studies under the direction of the Clinical Research Manager (CRM) and oversight of the Principal Investigator (PI). The CRC may be involved in the coordination and administration of FDA-regulated clinical trials (Phase 2-4), other sponsored studies or registries, and investigator-initiated studies related to urologic care, especially in the areas of urinary incontinence and cancer of the prostate, bladder, and kidney. The CRC must be able to effectively coordinate multiple studies concurrently and appropriately prioritize tasks across assigned studies and responsibilities.
Qualifications
Bachelor's degree in health/medical or biological science field is highly preferred.
Current (non-expired) Good Clinical Practice (GCP) training documentation is preferred. Current GCP training with FDA-focus required within the first 2 weeks of hire.
Certification in clinical research (e.g., CCRC, CCRP, or CRA) is preferred.
Minimum of three years of full-time experience or equivalent:
Biomedical or clinical research
Clinical care or laboratory medicine (e.g., MA, LPN, RN, MLT)
Research or clinical/healthcare administration *Partial years and/or part-time experience may be added together to a total of 3 years. Having an advanced degree in a health- or science-related field will qualify as one year of experience.
Prior experience working within an electronic medical record (EMR) system is highly preferred.
Primary Responsibilities
Study preparation and planning
Acquiring and filing/maintaining regulatory documents and other documentation
Regular and timely communication with stakeholders
Tracking of study- and patient- related information and status in spreadsheets/databases
Maintenance and tracking of supplies, equipment, and investigational products/devices/drug
Patient recruitment, prescreening, and consenting
Benefits
Comprehensive benefits package for full time employees
Medical, Dental, Vision and much more
Opportunities for career advancement
401k plan with employer match
PTO/Vacation
Minnesota Urology P.A. is an equal opportunity employer.
For more information, or to apply now, you must go to the website below. Please DO NOT email your resume to us as we only accept applications through our website.
https://www.applicantpro.com/j/3159619-342274
Refer to ID 3159619 when applying |
|