Clinical Research Coordinator- Clinical Assistant

Minnesota Urology•Bloomington, MN

1d•Onsite

About The Position

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. At MNU, we share the value of transparency and enable this during our recruiting process. We believe it's important to share the compensation range to best understand the full opportunity of a role! We select our initial range based on reliable compensation survey data. Other factors we consider in setting the specific pay for an individual will generally include, among other things, experience, specialized skills, work location, and internal equity to provide competitive offers. The range stated below is a starting point of the compensation conversation, we'd like to hear what your compensation expectations are too!

Requirements

RN, LPN or Medical Assistant in a clinical setting (especially oncology) experience.
Passion to advance your career into the research field.

Nice To Haves

Experience in clinical or biomedical research, healthcare or laboratory medicine, clinical research coordination, and/or healthcare administration.
Background in oncology or genitourinary cancers.
Familiarity with EMR systems, regulatory guidelines, and Good Clinical Practice (GCP).
Relevant certifications such as CCRC, CCRP, or CRA.
A degree in a health, medical, or biological science field.
Highly organized.
Able to work independently while collaborating effectively with cross-functional teams.
Capable of managing multiple priorities across clinic locations.
Strong communication, problem-solving, and process improvement skills.
Ability to adapt to evolving protocols and regulatory requirements.

Responsibilities

Coordination of clinical research studies under the direction of the Clinical Research Manager (CRM) and oversight of the Principal Investigator (PI).
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.
Effectively coordinate multiple studies concurrently and appropriately prioritize tasks across assigned studies and responsibilities.