Clinical Research Nurse Coordinator

Company Name:
SCL Health
This position has responsibility to manage the initiation and maintenance of clinical trials, according to regulatory and institutional guidelines and requirements.
Reviews and implements new clinical trials. Ensures informed consent process has occurred and is properly documented.
Ensures compliance in all regulatory fields affecting the program. Obtains appropriate authorizations and completes all data resource documentation prior to randomization. Assures compliance with protocol details completes necessary records, coordinates scheduling of subject, monitoring visits and adverse events.
Educates patients, ancillary departments and staff to maintain protocol.
Enters and monitors data entry to research database in timely and accurate fashion. Continuous data collection regarding clinical trial patients after closure of studies.
Maintains IRB correspondence and meets renewal, amendment and/or expedited review requirements.
Plans and implements patient care according to protocol and standard of care. Identifies and assesses potential study candidates.
Reviews protocol inclusion/exclusion if occurred.
Maintains appropriate "shadow chart" patient information for auditing purposes.
Coordinates with pharmacy staff and dispensing as study medications. Assures proper documentation of medication dispensed.
Graduate of an accredited School of Nursing, required
Valid license as a Registered Nurse in the State of practice, required
Excellent communication and interpersonal skills, required
ACRP (Association of Clinical Research Professionals) or SoCRA (Society of Clinical Research Associates) Certification, preferred

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