Clinical Research Nurse- PRN

Reposted 9 Days Ago
Be an Early Applicant
Murfreesboro, TN, USA
In-Office
Mid level
Healthtech • Professional Services • Pharmaceutical
The Role
Manage unblinded clinical trial pharmacy responsibilities including preparation and dispensation of investigational IV and SC medications, ensure chain of custody and protocol compliance, travel to sites ~2-3 days/week, complete regulatory training and documentation, and provide professional patient and team support.
Summary Generated by Built In

Description

We are an equal employment opportunity employer and will consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability.

Our vision is to provide the best Rheumatology care, anywhere and, to balance sustainable operation with the highest possible level of patient care. We are a seeking an ambitious, friendly, positive, and compassionate Clinical Research Nurse to join our Research department.

The Clinical Research Nurse (CRN) reports to the Director of Research and is responsible for managing assigned unblinded protocols in compliance with Protocol, FDA CFR, GCP and company SOPs. The CRN will work independently as primary pharmacy designee for unblinded clinical trials in Arizona. The CRN will travel to all sites as needed to prepare investigational medication for subcutaneous injections or intravenous infusions. The CRN will also attend meetings, monitoring visits and has the opportunity to work from home when not needed on site.

Responsibilities:

  • Manages all assigned clinical trials unblinded pharmacy responsibilities
  • Travels to sites approximately 2-3 days per week to prepare investigational medication 
  • Responsible for preparation of unblinded clinical trial medications for IV Or SC administration.
  • Performs dispensation of investigational product (IP) using web-based drug dispensation transactions
  • Ensures correct dose and medication is prepared for each subject visit
  • Perform subcutaneous administration for unblinded trials
  • Responsible for the chain of custody and accurate accountability of investigational products and devices
  • Ensures uniform implementation of protocols by completing the required training documentation in a consistent, accurate and timely manner.  
  • Performs all functions according to established policies (SOPS), procedures, regulatory and accreditation requirements, as well as applicable professional standards. 
  • Provides all employees and research subjects with excellent service experience by consistently demonstrating professional decorum.

Requirements

Minimum Qualifications:

  • Licensed Registered Nurse (RN) or Licensed Practical Nurse (LPN)
  • Infusion experience preferred
  • Clinical research experience preferred
  • Possess strong organizational skills 
  • Maintains confidentiality of patient and study information
  • Excellent verbal and written communication skills 
  • Reliable method of transportation 

Skills Required

  • Licensed Registered Nurse (RN) or Licensed Practical Nurse (LPN)
  • Infusion experience
  • Clinical research experience
  • Strong organizational skills
  • Maintain confidentiality of patient and study information
  • Excellent verbal and written communication skills
  • Reliable method of transportation
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The Company
HQ: Phoenix, AZ

What We Do

Arizona Arthritis & Rheumatology Associates (AARA) is the largest private practice rheumatology group in the US, specializing in the management of autoimmune and rheumatological conditions. They also participate in clinical trials for new treatments.

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