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

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