Location : Fort Worth, TX

Hours/Schedule :

• Monday–Friday (7:30 AM–4:00 PM or 8:00 AM–5:00 PM) for the first 90 days.

After 90 days, flexible options include:

• 4 days/week, 10-hour shifts OR 9-hour shifts with every other Friday off.
• Remote Work: One day per week, depending on the schedule.

Employment Type : Contract-to-Hire (CTH)

Qualifications

Education :

• Bachelor of Science in Nursing (BSN) required.

Experience :

• Minimum of 3 years in nursing, with preference for ICU, ER or high acuity specialties.
• Oncology and/or research experience is highly desirable but not required.
• Experience in a clinic setting and demonstrated ability to collaborate with physicians daily.

Position Overview

Join a collaborative and dynamic oncology research team specializing in lymphoma and leukemia studies. As a Clinical Research Nurse (CRN) , you will play an integral role in managing clinical trial operations, collaborating with the care team, and ensuring high standards in research protocols and patient care. This position does not involve patient recruitment but emphasizes study start-up processes, protocol management, and team collaboration.

Key Responsibilities

Study Management :

• Oversee study start-up activities, including reviewing protocols and creating source documents.
• Collaborate with Clinical Research Coordinators (CRCs) to ensure study processes align with regulatory standards.

Documentation & Compliance :

• Review and manage Adverse Events (AEs) and Serious Adverse Events (SAEs).
• Maintain detailed and accurate study records in EPIC EMR (prior experience with EPIC is a plus).

Monitoring & Communication :

• Participate in monitoring visits and address feedback from monitors and investigators.
• Foster daily communication and relationships with physicians (12 Principal Investigators and 6 Sub-Investigators).

Team Collaboration :

• Work alongside 4 RNCs, 3 CRCs, and 1 Data Manager on the Oncology team.
• Contribute positively to a strong and cohesive team dynamic.

Training and Onboarding

• Comprehensive 3-week training program, ensuring you are fully prepared before transitioning to onsite responsibilities.
• Structured mentorship and guidance to familiarize you with the organization's research protocols and workflows.