Rn Nurse - Research

Job Title:

Registered Nurse (RN) / Clinical Research Coordinator - Research

Salary Range:

$37.86 - $50.48

Worker Category:

Full-Time

FLSA Classification

Non-Exempt

Department & Location:

Clinical Research 8280 Santa Monica Blvd

Organization Background

Men’s Health Foundation connects men at risk to comprehensive healthcare and wellness through education, collaboration, and advocacy. Inspiring and empowering all men to live longer, healthier, and happier lives. We see a world where inequity and stigma do not separate men from healthcare. At Men’s Health Foundation, we are reimagining men’s healthcare.

Founded in 1999, Mills Clinical Research conducts cutting-edge research with a special focus on infectious diseases including HIV prevention and treatment, vaccine trials, medical device trials, and trials focused on men’s health. Mills Clinical Research is led by Dr. Anthony Mills as the CEO and Primary Investigator (PI) with office locations in West Hollywood and South LA. MCR is affiliated with Men’s Health Foundation and has expansive community networks within Southern California. They share the mission to eliminate health inequity for all, especially those at risk.

Job Description

Overview

The Clinical Research Registered Nurse role is integral in the execution of clinical research trials and managing patients' individualized health plans to facilitate the progress of research studies. This includes assisting in patient recruitment, conducting clinical assessments, participating in research protocols, administering investigational treatments, and ensuring compliance with ethical and regulatory standards.

The RN will work under the guidance of the Principal Investigator, Sub-Investigators, and/or Director/Manager of Clinical Research Operations to participate in the planning, implementation, and overall direction of clinical research projects conducted on behalf of the sponsors at the institute. You will perform study procedures, transcribe source data to case report forms, and liaise with sponsor personnel, maintaining a high level of professional expertise through familiarity with the study protocol, investigator’s brochure, related study materials, standard operating procedures and policies, and participation in project team meetings. Ensuring research quality by practicing compliance and following the principles of Good Clinical Practice (GCP)/International Harmonization Conference (ICH), Health Insurance Portability and Accountability Act (HIPAA), Federal Drug Administration (FDA) policies and guidelines, and other applicable regulations (state and local).

Essential Functions and Responsibilities (This list may not include all the assigned duties)