Clinical Research Nurse

Overview

At Rose Research Center, we hope it is a wave of the future that inhaling combustible burning tobacco will someday be a thing of the past.

Welcome to a new career path with Rose Research Center!

Ready to be aClinical Research Nurse for our clinical team?

Who are we?

Rose Research Center (RRC) is a private research company specializing in nicotine and tobacco research. In the field of nicotine, smoking cessation, and harm reduction research we pride ourselves on being some of the best in the industry. Our leadership team brings over 100 years of industry leading experience from their respective careers. Our CEO, Dr. Jed Rose, is recognized internationally for his contributions to this space including, but not limited to, the co-invention of the nicotine skin patch, inspiring the development of Chantix, among countless others.

What do we do?

We research new methods to save lives. RRC is a leader in the field of nicotine research. We work with the National Institutes of Health, Pharmaceutical partners, Industry partners, small businesses, non-profit organizations, and others to find an end to addiction of combustible nicotine products.

The primary responsibilities of this position are to perform peripheral IV catheter placement and execute highly accurate, time-point-driven blood draws according to the study's Pharmacokinetic Sampling Schedule by collecting samples within narrow, pre-defined windows (e.g., ±1 minute). The ideal candidate will follow strict lab manual protocols, process, handle, and store biological specimens (e.g., whole blood, plasma, serum) including:

• Centrofuging samples at required speeds and temperatures
• Pipetting and aliquoting plasma/serum into labeled cryovials.
• Immediate and meticulous labeling, inventory documentation, and storage of samples at specified temperatures until shipment.

The Clinical Research Nurse will also perform and document other protocol-required clinical assessments, including vital signs, and focused physical assessments. They will continuously monitor study participants during and after dosing/sampling periods for signs of adverse events (AEs) or complications related to procedures, or study participation, and report all findings promptly to the Principal Investigator or designee.

In this position you will:

• Follow guidelines for Good Clinical Practice based on the current International Conference on Harmonisation (ICH) and the corresponding sections of the United States Code of Federal Regulations governing Protection of Human Subjects (Title 21 CFR Part 50), Institutional Review Boards (Title 21 CFR Part 56), the Basic Principles of the Declaration of Helsinki, and applicable legal and regulatory requirements.
• Independently perform venipuncture for the insertion of peripheral IV catheters (e.g., indwelling cannulas) in study participants for the purpose of collecting blood samples.
• Execute highly accurate, time-point-driven blood draws according to the study's Pharmacokinetic Sampling Schedule. This includes collecting samples within narrow, pre-defined windows (e.g., ±1 minute).
• Following strict lab manual protocols, process, handle, and store biological specimens (e.g., whole blood, plasma, serum).
• Perform and document other protocol-required clinical assessments, including vital signs, and focused physical assessments.
• Continuously monitor study participants during and after dosing/sampling periods for signs of adverse events (AEs) or complications related to procedures, or study participation. Report all findings promptly to the Principal Investigator or designee.
• Accurately and contemporaneously record all clinical data, procedures performed, exact time points of blood draws, and observed participant responses in source documents and electronic Case Report Forms (eCRFs).
• Ensure all clinical procedures, including the Order of Draw and specimen processing steps, strictly adhere to the study protocol, FDA regulations, and Good Clinical Practice (GCP) guidelines.
• Manage and maintain inventory of clinical supplies, including IV start kits, phlebotomy supplies, specimen kits, and investigational product accountability.
• Assist in the…