RN, Clinical Research Job at CARTI, Little Rock, AR

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  • CARTI
  • Little Rock, AR

Job Description

Join to apply for the RN, Clinical Research role at CARTI .

Brief Description

The RN, Clinical Research executes and coordinates daily clinical research activities according to GCP and FDA/ICH guidelines; reviews and assists in the selection of sponsor-supported clinical trials; completes and organizes all IRB/Sponsor regulatory documents; negotiates clinical trial budgets and invoices for site activities; ensures IRB-approved protocols are implemented and followed; educates patients and their families about clinical trial treatments and possible side effects; executes and documents the informed consent process and monitors patient status and safety; collects, organizes and reports research data; schedules and conducts study-specific training and site in-services to study-related staff on new or amended protocols; conducts visits with CRAs (Clinical Research Associates) to initiate protocols and to verify source documents; maintains investigational product inventory and oversees the dispensing of investigational product to patients; reports regularly to the Principal Investigator on the status of all open clinical trials under his/her supervision. Works closely with the laboratory to ensure samples are collected and processed according to protocol.

Responsibilities


  • Enlist, maintain, and assure protocol compliance for all patients on clinical trials.
  • Collaborate with physicians to determine eligibility of patients for clinical trials.
  • Practice in compliance with SOPs, GCP, and applicable federal, state, and local regulations.
  • Screen potential patients for protocol eligibility; present trial concepts and details to the patients; participate in the informed consent process; enroll patients on protocol.
  • Coordinate patient care in compliance with protocol requirements; may disburse investigational drug and provide patient teaching regarding administration; maintain investigational drug accountability.
  • Review patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly document all findings.
  • Accurate and timely data collection, documentation, entry, and reporting; schedule and participate in monitoring and auditing activities.
  • Maintain regulatory documents in accordance with SOPs and applicable regulations.
  • Participate in required training and education programs; educate clinic staff regarding clinical research.
  • Additional responsibilities may include working directly with other research bases and/or sponsors.
  • Provide a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC.
  • Interact with the Clinical Trial Sponsors to recruit new clinical trials for the site; conduct feasibility questionnaires and participate in site selection process.
  • Negotiate the clinical trial budget with the Sponsor and invoice for the completed site activities.
  • Order and maintain inventory of all study-specific supplies including recruitment materials and specific lab kits.
  • Collect, process and ship all study-defined lab kits to the Central Lab as directed by the sponsor.


Qualifications
  • Graduate from an accredited school of nursing.
  • Associates degree or equivalent from a two-year college program, technical school, or nursing diploma.
  • Bachelors degree, preferred.
  • Current registered nurse licensure in Arkansas.
  • BLS certification.


Experience, Knowledge, Skills & Abilities
  • Two or more years of experience in clinical research or oncology, preferred.
  • Proficiency with Microsoft Office applications (Outlook, Word, Excel).
  • Detail oriented, organized, self?motivated, able to work independently and on a team.
  • Excellent communication, teamwork and problem?solving skills.
  • Professional, high work ethic, strong work ethic, ability to adapt to additional tasks.
  • High integrity and ability to maintain confidentiality.


Other Requirements
  • Occasional travel to satellite clinics.


Seniority Level
  • Entry level


Employment Type
  • Full?time


Job Function
  • Health Care Provider
  • Hospitals and Health Care industry



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Job Tags

Full time, Work at office, Local area,

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