RN/BSN Clinical Research

RN/BSN

 

Clinical research exp preferred, but not required for Adult/Ped allergy/asthma/immunology clinical research ctr near St. Joe’s. Research Director on site. Excellence in GCP’s, Pl supervision, flex hrs, occ ev/wk ends. Pleasant work env/stable staff. Competitive salary, bonus, health insurance, 401K.







CLINICAL RESEARCH NURSE COORDINATOR



Job Title: Clinical Research Coordinator (CRC) RN

Reports To: Director of Clinical Research

 

Job Summary:

Perform all clinical nursing and coordination responsibilities related to Center’s research trails, under the supervision of the Research Center Director and Principal Investigator.

 

Job Requirements: Current Georgia RN License BSN degree preferred 2 years minimum experience in clinical research Pediatric medical care experience CRC-certified or willing to become CRP-certified IV Infusion Skills Working knowledge of one or more aspects of clinical trials (GCP) research: including data collection, analysis, or monitoring; case management of protocol participants; recruitment and enrollment; protection of subjects and subjects’ rights through IRB relations; development of informed consents; preparation of adverse event experience reports; construction or monitoring of case report forms; maintenance of drug accountability records; grant and budget development; report preparation; education of other health-care professionals, patients or families regarding clinical trials, protocol development, program administration; and research program audit.

 

Job Duties & Responsibilities: Conduct clinical trials according to FDA regulations and guidelines. Design and maintain organizational tools to conduct trials accurately and in compliance with GCP and Protocols. Ensure the safety and welfare of the study participants. Adhere to the Sponsor’s protocol to ensure all study activities are completed accurately and completely. Train other site personnel and other medical staff to understand and implement the protocol. Recruit and screen potential study participants according to the protocol’s inclusion and exclusion criteria. Obtain proper written informed consent from each study participant prior to participation in the study. Schedule study participants’ visits and perform defined activities of the study completely and accurately, during the study participant’s visit. Report, immediately, all adverse events to the investigator and Clinical Research Director. Maintain complete and accurate case report forms (CRF) and source documents for each study participant and record pertinent observations and data during the study. Communicate with the Sponsor regarding study activities as necessary. Meet with the Sponsor’s representatives to discuss the conduct of the study and review study data. Attend Coordinator Meetings (as required) to learn study requirements, meet sponsor personnel, represent the site and convey all information to the site study-team upon return (some travel required). Maintain IRB-related records and communications. Other research-related duties as assigned by Clinical Research Director and/or Principal Investigator.