Clinical Research Nurse - 249448 Job at Medix™, Nashville, TN

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  • Medix™
  • Nashville, TN

Job Description

Overview

We are seeking a dedicated Clinical Research Nurse to support oncology clinical trials in a patient-facing research environment. This role plays a critical part in coordinating study activities, ensuring protocol compliance, and providing education and support to study participants throughout the research lifecycle.

Key Responsibilities

  • Coordinate and manage patient participation in clinical research studies, including recruitment, screening, enrollment, treatment administration, and follow-up in accordance with study protocols.
  • Educate participants on study procedures, expectations, and responsibilities to ensure informed and compliant participation.
  • Obtain, document, and maintain informed consent and HIPAA authorization, ensuring accuracy and ongoing compliance.
  • Review study protocols and eligibility criteria with investigators and participants.
  • Prepare, complete, and submit study documentation and case report forms within required timelines.
  • Maintain accurate and complete source documentation, including clinical data, visit notes, and participant outcomes.
  • Evaluate new and returning patients, review diagnostic imaging or scan results, and track eligibility and study status.
  • Provide ongoing oversight of participants to ensure subject safety, protocol adherence, and data quality.
  • Verify required approvals prior to treatment initiation or medication changes, including protocol-mandated dose adjustments or crossover.
  • Dispense oral investigational products and educate participants on proper administration.
  • Perform and document protocol-required clinical calculations (e.g., BSA, creatinine clearance, urine protein-to-creatinine ratios).
  • Coordinate and schedule study visits, labs, imaging, and other protocol-required procedures.
  • Identify, document, and report adverse events and safety findings per protocol and regulatory requirements.
  • Complete study discontinuation documentation when applicable.
  • Facilitate participant re-consent when updated informed consent forms are issued.
  • Maintain investigational product accountability, including inventory management and reconciliation.
  • Collaborate closely with investigators and research staff to meet study goals and timelines.
  • Serve as a primary liaison between study participants, investigators, and the research team.
  • Provide coverage or support at additional research sites as needed.

Required Qualifications

  • Active RN license
  • Associate’s Degree in Nursing
  • Minimum 1 year of oncology experience
  • 2 years of clinical research experience

Schedule

  • Monday–Friday, 8:00 AM–5:00 PM
  • Flexibility available based on patient visit schedules

Why Join Us?

  • Growing research team with opportunities for upward mobility
  • Hands-on involvement in meaningful oncology clinical trials
  • Collaborative, patient-centered research environment

Job Tags

Monday to Friday,

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