Clinical Research Coordinator at Minnesota Urology PA
Woodbury, MN 55125, USA -
Full Time


Start Date

Immediate

Expiry Date

11 Oct, 25

Salary

36.38

Posted On

13 Jul, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Care, Clinical Research, Training Documentation, Research, Laboratory Medicine

Industry

Pharmaceuticals

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.

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

How To Apply:

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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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