Job Description

Highlights

• $60 - $65/hr
• Great benefits including 401k w/match and 15 days PTO
• Stepping stone into clinical research based roles!
• Work on cutting edge oncology 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.

Responsibilities

• A dhere to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements.
• Perform IV infusions of both blinded and unblinded investigational products in accordance with study protocols.
• Obtain blood specimens and other biological samples from study participants using proper clinical procedures.
• Ensure accurate, complete, and timely source documentation in compliance with GCP and sponsor guidelines.
• Monitor study participants for adverse events and report findings in accordance with study protocols and regulatory requirements.
• Maintain the confidentiality, security, and integrity of study data and participant information.
• Collaborate effectively with investigators, study coordinators, and other clinical staff to ensure protocol adherence.

Qualifications:

Education

• Licensed Practical Nurse (LPN) or Registered Nurse (RN) with a current, active license.
• Experience administering chemotherapy
• IV infusion experience
• Strong computer proficiency, including Office 365 products.
• Flexible and adaptable to occasional long shifts, night shifts, or overnight shifts

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