Clinical Research Nurse (Part Time) in Grayslake, IL

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  Job Description

Job Title: Research Nurse II

Part-time (M-F 7 am to noon) an occasional Saturday or evening shift during the weekend).  Training will be on the same schedule

RN licence needed
 
2 yrs exp needed
 
Some one who is available to work in mornings (4-5 hours can be more) (must have)
 
Some one who is flexible with occasional Saturday or evening shift if needed (not a must have)
 
Candidate should be flexible with shift timings
 
Flexible to accommodate for afternoon hours if needed
  • Should be able to do administrative work in the backend
  • Tech savvy
  • Disburses investigational drug and provides teaching regarding administration
  • Interfaces with research participants to support efforts to determine eligibility and consenting of study participants according to protocol. Review and assess data collected.
  • Give instructions to patients regarding what to eat or drink, what not to eat or drink during trials period
  • Nurse engaged in the practice of care/assessments of the healthy volunteers and/or patient.
  • Some exp with clinical trials
  • Assists with the execution of study-related activities of a Phase I clinical research study. Research nurses should primarily be concerned with the protection and care of research subjects.
  • Participate in the recruitment and screening activities to ensure successful enrollment of volunteers into studies scheduled at the Phase 1 Unit.
  • Some one who can multitask
  • Take nasal covid swabs
  • Quick learner
  • Associates degree needed minimum

100% Onsite

Purpose

  • The Clinical Research Nurse is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI).
  • Assists with the execution of study-related activities of a Phase I clinical research study. Research nurses should primarily be concerned with the protection and care of research subjects.
  • The primary role is to function as a licensed registered nurse engaged in the practice of care/assessments of the healthy volunteers and/or patient.
  • Position includes disseminating information regarding new information for documentation, performance improvement and data source upgrades.

Responsibilities

  • Review protocols and informed consent forms for scheduled studies, identify and communicate potential issues to the appropriate personnel.
  • Participate in nursing study related activities as required by protocol compliance with Corporate, divisional, and departmental SOP’s and external (CFR, ICH GCP) regulatory guidelines.
  • Responsible for compliance with applicable Corporate and Divisional Policies and Procedures.
  • Evaluate adverse events and manage safety reporting activities in a timely manner.
  • Interact with the Principal Investigator and other study physicians, Recruiting/Screening, Data Systems, and other personnel in support of study-specific activities.
  • Support quality and compliance improvement initiatives as appropriate.
  • Participate in the recruitment and screening activities to ensure successful enrollment of volunteers into studies scheduled at the Phase 1 Unit.
  • Interfaces with research participants to support efforts to determine eligibility and consenting of study participants according to protocol. Review and assess data collected.
  • Serve as a resource person or act as a consultant within area of clinical expertise (R/S).
  • Disburses investigational drug and provides teaching regarding administration, as necessary. Develops accurate source materials and ensures compliance from site staff. Ensures all protocol procedures are completed per study requirements (Unit).
  • Other tasks as assigned.

 What are the top 3-5 skills, experience or education required for this position:

  • Required Skill 1: Communication skills
  • Required Skill 2: Listening and answering volunteer questions
  • Required Skill 3: Customer Service skills
  • Required Skill 4: Multitasking
  • Required Skill 5: Nursing skills


About Rangam:

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