Clinical Research Coordinator Fort Collins and Greeley

Primary City/State:

Fort Collins, Colorado

Department Name:

Research

Work Shift:

Day

Job Category:

Research

Estimated Pay Range:

$27.16 - $40.22 / hour, based on location, education, & experience.

In accordance with State Pay Transparency Rules.

A rewarding career that fits your life. Those who have joined the Banner mission come from all walks of life, united by the common goal: Make health care easier, so life can be better. If changing health care for the better sounds like something you want to be part of, apply today.

Located just 45 minutes north of Denver, Northern Colorado offers trendy restaurants, a thriving retail sector, and endless cultural amenities. Between wildflower-filled meadows and spectacular views of the Rocky Mountains, you will find adventures by horse, mountain bike and boat plus, endless hiking trails and world class skiing.

We currently have a full-time opening, as a Clinical Research Coordinator supporting two of our Orthopedics locations. This is an on-site role, where you will be responsible for enrolling patients in our current Orthopedic studies, having consenting conversations with eligible patients, along with collecting and organizing the data of the study. This position will work closely with the physicians overseeing the study. The preferred candidate will have prior experience in research.

Location:

Will float between the following clinics throughout the week:

• Banner Health Clinic--Orthopedics 5890 W 13th St, Ste 101 Greeley, CO 80634
• Joint Replacement Center 702A W Drake Rd Fort Collins, CO 80526
  
  

Shift:

Monday - Friday, 8am - 5pm

See the Benefits Guide under the Total Rewards section of this posting, to learn more about our great benefit package!

If interested, apply today!

Banner Fort Collins Medical Center is built on a 28-acre campus, is a 29-bed facility and a level IV trauma center. The state-of-the-art, two-story facility features a 24-bed inpatient unit, emergency department, lab services, labor and delivery rooms, medical imaging, surgical services and women's services. The campus also includes an outpatient clinic. Banner Health was recognized by Becker’s as a Top 150 Places to Work in Healthcare in 2023.

Position Summary

This position is responsible for coordinating and/or implementing assigned protocols. This position includes collecting and recording medical data and history, assisting in patient assessments, and maintaining study files.

Core Functions

• Provides study information and obtains relevant information to and from patients engaged in clinical studies, which includes: assisting in the recruitment and screening of volunteers; registering patients; providing information on clinical trials and protocols to interested participants in a timely and helpful manner; obtaining relevant medical history on candidates by phone and in person; collecting previous relevant medical records data on patient; explaining procedures and consent forms; compiling all information prior to the initial visit; responding to inquiries from study participants or collateral informants in a timely and helpful manner; updating databases with patient information; and/or, performing other related activities.
• Performs tasks required by protocol, which may include obtaining patient medical history, systems review, phlebotomy, EKG, and cognitive assessment on patients. Collects vital signs. Maintains quality assurance on designated protocols. Collects data as required and assists in interpreting and evaluating results as required.
• Triages adverse events and communicates with the research physician regarding the occurrence of adverse events. Collects information regarding indicated medical follow-up with the subject and collateral informants as needed.
• Provides educational information to patients and their families. Serves as a resource and support person for patients and families by being a consistent person they can contact within the clinical research program. Provides information to the patient and family related to the healthcare of the patient such as health maintenance, prevention, and anticipatory guidance relevant to study-related diseases.
• Ensures uniform implementation of protocols by completing required documentation in a consistent, accurate and timely manner. Assists in preparing appropriate IRB (Institutional Review Board) forms, informed consents, correspondence with sponsor, etc., in an accurate and timely manner. May participate in the annual IRB approval and update process.
• Serves as a liaison to other departments and programmatic areas, as well as community agencies.
• Ensures that primary referring physicians receive timely progress notes on the patient’s diagnosis and treatment.
• May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.
• Department level responsibility. Some positions may have frequent interaction with patients, families, visitors, physicians, and related clinical departments.
  
  

Minimum Qualifications

Must possess knowledge of clinical research methodologies as normally obtained by the completion of a bachelors' degree in a healthcare field.

Experience typically gained through two to four years clinical research experience. Familiarity with medical and clinical terminology. Must have excellent organizational and task management skills. Ability to maintain confidentiality of patient and study information. Ability to maintain knowledge of Federal and State regulations governing practice as well as Institute policies and procedures related to medical and nursing practice. Excellent human relations, organizational and communication skills are required.

Preferred Qualifications

Possession of Clinical Research Coordinator Certification (CRCC).

Additional Related Education And/or Experience Preferred.

Anticipated Closing Window (actual close date may be sooner):

2026-03-25

EEO Statement:

EEO/Disabled/Veterans

Our organization supports a drug-free work environment.

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