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Nurse Practitioner; Clinical Research

Job in Los Angeles, Los Angeles County, California, 90079, USA
Listing for: SQRL
Full Time position
Listed on 2026-01-11
Job specializations:
  • Science
    Clinical Research
Job Description & How to Apply Below
Position: Nurse Practitioner (Clinical Research)

Associate Director of Recruiting at SQRL

This role is focused exclusively on Oncology Clinical Research Trials.

Highlights
  • 401k with match
  • 15 days PTO
  • 10 paid holidays
  • Great benefits including 401k with match, 15 days PTO, 10 paid holidays, and more
  • Focus exclusively on Oncology Clinical Research Trials
About Our Client

Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best‑in‑class experience for patients and sponsors.

The Role

The Sub-Investigator (Clinical Research NP) is responsible for oversight and execution of clinical trials that test new medications on behalf of sponsor/pharmaceutical companies. You will work in an oncology clinic to promote Good Clinical Practice and follow research protocols assigned alongside the PI. You will work along a lead Physician (Principal Investigator) have a team of skilled coordinators, managers, and assistants as well.

Responsibilities
  • Evaluate and screen potential subjects based on study eligibility criteria
  • Perform and review medical procedures in accordance with the clinical study protocol
  • Complete all documentation, paper and electronic
  • Provide oversight and ensures proper delegation of duties to appropriate staff

    Provide and maintain updated study related documentation
  • Evaluate and report safety reports, protocol noncompliance and any other protocol specific reports.
  • Medical management of patients on trial
  • Administering medications including IV
  • Tracking and management of adverse events
  • Monitoring
Qualifications
  • Ability to dedicate a full time schedule on site in Century City, CA
  • Prior experience working with Oncology research
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