RN - Clinical Research Float - FT

RN - Clinical Research Float - FT

Shift: Monday-Friday, 8:00a-5:00p (with some flexibility)

Primary location:
Sayre, PA, Additional locations Corning, NY and Binghamton, NY

On Call:
Every 9th-10th week, may include weekend

Up To $25,000 Sign On Bonus For Qualified RNs!

Coordinate multiple in-patient and out-patient clinical research protocols. This coordination requires extensive knowledge forthe disease pathophysiology, pharmacology treatments, patient disease evaluation workflow, and the ability to collaborate and communicate new processes related to research with the involved departments.

The RN Clinical Research must be licensed in both Pennsylvania and New York. The applicant must have a current license as a Professional Registered Nurse in PA prior to position start date. Additional NY state licensure must be obtained within 3 months of hire. Patient outreach and contact will be limited to those patients living in the state of current licensure until dual licensure is obtained.

"Musthave aRegistered

Nursing license in PA and NY
** andmeetoneofthefollowing:

Experience:

Desire certification in the disease specialty being studied or as a Clinical Research Professional. Three years full time experience in the nursing field required. Experience successfully leading or advancing a project with peers, leadership, and/or external customers.

Coordinate individual clinical research projects in multiple disease conditions.

Project coordination requires meeting sponsor specific training requirements prior to initiation, assuring team members have met sponsor training, training team members to delegated duties, supporting regulatory specialist with sponsor communications, maintaining study supply inventory, and supporting monitors during visits. Each project requires institutional process development strategies.

This research team member develops or advances the investigators plans.

Collaborate with the manager and executive director for the development of department research programs. This is demonstrated through advancing research meetings in the Guthrie Medical Group departments. These meetings communicate the performance metrics regarding enrollments, training requirements and new protocol opportunities.

Additional responsibilities for specific program development include assisting with feasibility, site selection, IRB document review, and corresponding with investigators, IRB, and sponsors.

This role coordinates the study protocol procedure events and treatment planning with the investigator.

This coordination for the patient includes reviewing medical history for eligibility, educating the patient to the study requirements, registering the participant to the project, and organizing patient visits.

Patient visits requirements involve scheduling, reviewing treatment plans, assuring study treatment and supplies are available and documenting the encounter.

This documentation must meet Good Clinical Practice standards of attributable, legible, contemporaneous, original, accurate, and complete.

Lastly follow-up with the participant related to next visit and study requirements.

Administering and dispensing investigational medication ordered forthat that patient by a licensed physician in the dosage prescribed by protocol.

Retrieval of medication and assessment of compliance by patient to the protocol.

Routine travel between Guthrie research sites may be required, as well as periodic travel for protocol training.

Collaborate with director, manager, research team members and IRB coordinator in developing and revising process flow for research procedures.

Attend training seminars and conferences as required by sponsor of research study.

Make presentations of study information to groups of physicians and patients. Assist physicians in protocol development.

Advise department manager on resource utilization and training needs.

Perform other duties as assigned by the director or manager.

The pay range for this position is $40.00 - $54.12 per hour.

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