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RN Nurse - Research

Job in West Hollywood, Los Angeles County, California, 90069, USA
Listing for: Men's Health Foundation
Full Time position
Listed on 2026-07-01
Job specializations:
  • Nursing
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below

Benefits

We recognize our staff as the heart of our organization and seek to provide a generous and competitive benefits package to support our employee's well‑being.

  • Medical, Dental, Vision, Life and LTD insurance (may be eligible on the 1st of the month following date of hire)
  • 12 Paid Holidays (including 1 mental health day)
  • 401(k) Retirement plan (may be eligible for employer matching up to 4% following completion of 90th day of employment)
  • Flexible Spending Account (FSA)
  • 40 hours of sick pay (following completion of 90th day of employment)
  • 120 hours of PTO accrued within the 1st year of employment

We seek team members who embrace and champion diversity; as our work within the LGBTQ+ community promotes positive sexuality and inclusivity, candidates should be comfortable with exposure to imagery, events, and materials that reflect our culture of acceptance and expression.

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 (MCR) 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. MCR is led by Dr. Anthony Mills as the CEO and Principal 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, sharing the mission to eliminate health inequity for all, especially those at risk.

Job Description Overview

The Clinical Research Registered Nurse (RN) plays a critical role in the successful execution of clinical trials at Mills Clinical Research (MCR). This role integrates clinical nursing practice with research operations to ensure the safe, compliant, and efficient conduct of studies while delivering high‑quality, patient‑centered care.

The RN is responsible for performing protocol‑specific procedures, supporting participant recruitment and retention, administering investigational products, and ensuring accurate and timely documentation of clinical and research data. This position works in close collaboration with the Principal Investigator (PI), Sub‑Investigators, and Clinical Research Operations leadership to support study implementation and ongoing trial conduct.

The Clinical Research RN maintains strict adherence to study protocols, Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, HIPAA, FDA regulations, and all applicable state and local requirements. Success in this role requires strong clinical judgment, attention to detail, operational efficiency, and the ability to function within a fast‑paced research environment.

Essential Functions and Responsibilities (This list may not include all duties assigned.)
  • Perform protocol‑required clinical procedures, including physical assessments, specimen collection, phlebotomy, injections, IV placement and administration, and preparation and administration of investigational products, in accordance with study requirements and physician orders.
  • Ensure accurate, timely, and complete documentation of all clinical and research activities in source documents, electronic health records, and case report forms (CRFs/eCRFs).
  • Support participant recruitment, screening, and enrollment by reviewing medical records, assessing eligibility criteria, and educating potential participants on study requirements.
  • Obtain and document informed consent in compliance with regulatory and ethical standards prior to initiation of any study‑related procedures.
  • Monitor participant safety by reviewing laboratory results, performing medication reconciliation, identifying, reporting, and promptly escalating adverse events and clinical concerns to the PI and Sub‑I.
  • Dispense investigational products in accordance with protocol, ensuring proper…
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