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Oncology Research Registered Nurse; RN - Northwest Houston, Tx

Job in Houston, Harris County, Texas, 77246, USA
Listing for: Maryland Oncology Hematology
Full Time position
Listed on 2026-01-24
Job specializations:
  • Nursing
    Oncology Nurse, Healthcare Nursing, RN Nurse, Clinical Research Nurse
Job Description & How to Apply Below
Position: Oncology Research Registered Nurse (RN) - Northwest Houston, Tx

Senior Oncology Research Registered Nurse (RN) - Northwest Houston, Tx

Join to apply for the Senior Oncology Research Registered Nurse (RN) - Northwest Houston, Tx role at Maryland Oncology Hematology.

Overview

Texas Oncology is looking for a Senior Oncology Research Registered Nurse (RN) to join our team in Northwest Houston, Texas. This is a full-time Monday – Friday position with no weekends, call, or major holidays.

At TxO – Houston Northwest locations, we bring advanced treatment and compassionate support close to home. Texas Oncology is the largest community oncology provider in the country with approximately 600+ providers across 300+ sites.

What does the Oncology Research Nurse (RN) do?

This position offers a unique opportunity to work as a nurse in oncology clinical research. As a Clinical Research Nurse, you will provide care for patients receiving cutting-edge treatments within the oncology clinic. This position provides a variety of responsibilities while developing rewarding relationships as you manage the cancer patient throughout their journey. Working in clinical research offers opportunities for professional development, tuition reimbursement, and an annual bonus for oncology certified nurses.

Supports and adheres to the US Oncology Compliance Program, including the Code of Ethics and Business Standards.

Responsibilities
  • Work closely with physicians to identify and screen potential patients for clinical trial participation
  • Present trial concepts and details to oncology patients while conducting the informed consent process
  • Assess patients for adverse events and/or changes in condition
  • Provide staff and patient education regarding the management and administration of investigational product
  • Ensure accurate and timely documentation and data entry to meet trial requirements
  • Serve as a liaison between clinic departments to ensure proper trial conduct
  • Oversees the preparation of orders by physicians to assure that protocol compliance is maintained
  • Enters orders to assure that protocol compliance is maintained
  • Responsible for compiling and reporting protocol activity, accrual data, and research financials to practice administration and physicians
  • May be responsible for the development of practice research budgets
  • Maintains regulatory documents in accordance with USOR SOP and applicable regulations
  • Participate in scheduling monitoring and auditing visits; interacts with the monitors/auditors onsite
Qualifications
  • Education/Training
    Graduate from an accredited program for nursing education required (BSN preferred);
    Current licensure as a registered nurse in state of practice;
    Current BLS certification required;
    Minimum one (1) year of nursing experience required, preferably in oncology;
    Experience in clinical research strongly preferred; OCN, SoCRA or ACRP certification strongly preferred
  • Level I
    • Graduate from an accredited program for nursing education required (BSN preferred)
    • Current licensure as a registered nurse in state of practice
    • Current BLS certification required
    • Minimum one (1) year of nursing experience required, preferably in oncology
    • Experience in clinical research strongly preferred
    • OCN, SoCRA or ACRP certification strongly preferred
  • Level II
    • Minimum three (3) years of nursing experience, oncology experience strongly preferred
  • Level Senior
    • Minimum seven (7) years nursing experience, including at least one year in oncology strongly preferred
    • Previous management and/or leadership experience
  • Specialized Knowledge/Skills
    • Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents
    • Ability to work independently, organize, prioritize, and follow through with results
    • Ability to solve practical problems and implement solutions
    • Strong ability multi-task
    • Excellent communication skills
    • Excellent time management skills
    • Strong interpersonal skills to interact with multiple people on many different levels
    • High level of attention to detail
    • Ability to work in a fast paced environment
  • Working Conditions
    • Environment (Office, clinic)
    • The work environment includes possible exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic
    • Physical requirements include lifting up to 40 lbs, standing and walking for extended periods, and full range of body motion

* Hot Job*

Seniority level
  • Mid-Senior level
Employment type
  • Full-time
Job function
  • Health Care Provider
Industries
  • Research

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