The Clinical Research Unit (CRU) is committed to providing investigators and their teams a research environment and broad range of services guided by good clinical practice. This contributes to the conduct of excellence in clinical and translational research. The unit equips investigators with essential tools and critical resources, while providing a highly efficient and flexible infrastructure that is sustainable through a comprehensive cost-recovery system.

Nursing Services

Our experienced team of clinical research nurses are specially trained to assist you in the conduct of your studies. The nursing staff has a breadth of clinical and research experience that encompasses clinical care on a continuum of healthy volunteers to intense disease processes. Our nursing practice is guided by scientific knowledge, standards of care and a code of ethics.

We facilitate new studies by working closely with the research nurse coordinators to meet the specific needs of each protocol. We also facilitate staff education by coordinating in-services and ensuring staff have the knowledge needed to effectively carry out a research protocol.

Services

  • Nursing assessment
  • Patient education
  • Treatment monitoring
  • Medication administration
  • Point-of-care testing
  • Intravenous therapy
  • Pharmacokinetic sampling
  • Cardiac & pulse oximetry monitoring
  • Phlebotomy services
  • Questionnaire administration

Fees

Access a list of CRU Nursing fees here (Blazer ID required).

Register

The first step in accessing CRU services is registering. The following information is required:

  • A completed Registration Form  
  • Human Subjects Protocol (approval may be pending — send stamped approval form when available)
  • Consent Form(s) (approval may be pending — send stamped consent form(s) when available)
  • Protocol (Grant application, sponsor protocol, study group protocol)

The registration form and accompanying documentation should be sent electronically to This email address is being protected from spambots. You need JavaScript enabled to view it..

Study Initiation

After registering, you will receive an official letter from us that details the services to be used and any requirements to initialize the study. This letter must be signed by the PI and returned to us before the study can begin (Step 2).

Study Implementation

The third step is to hold an inservice for CRU nurses. An inservice should be scheduled at least two weeks prior to the first scheduled participant appointment. Email This email address is being protected from spambots. You need JavaScript enabled to view it. or call 205-975-2762 to schedule your inservice. To better understand the goals of an inservice, you may wish to review these Inservice Guidelines.

Scheduling Participants

After the inservice is completed, you can begin scheduling participants to receive CRU services. Call 205-934-7817 or email CRU Nurse Manager Jolene Lewis to schedule appointments for participants. A series of visits may be scheduled at one time to ensure availability of resources.

Outpatient: 15th floor of Jefferson Tower (625 19th Street S.).
Inpatient: 8th floor Medical Education Building (1813 6th Ave. S.).

Coordinator Tools

We offer several helpful tools for study coordinators. Available on request.

  • Coordinator Checklist
  • IV Infusion Sheet
  • Oral Drug Flow Sheet
  • OGTT Flow Sheet

Don't see what you need? Have an urgent request? Contact us at This email address is being protected from spambots. You need JavaScript enabled to view it. or 205-934-7442.

  • "Without the CRU these studies would not possible. Most of these studies involve the preparation of diets of known composition and this cannot be performed in a laboratory setting."


    — Ross P. Holmes, PhD, Professor, Department of Urology, UAB

  • "Controlled dietary studies are needed for such research, and would not be possible without the current infrastructure at UAB."


    — John Knight, PhD, Assistant Professor, Department of Urology, UAB