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.
Ability to manage multiple projects and work autonomously.
Strong problem solving skills.
Ability to communicate and collaborate with cross functional teams

Primary Responsibilities

Study preparation and planning. Clinical trial coordination including data collection and management
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

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Clinical Research Coordinator