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

Position Summary: 

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

Education, License & Cert: 

Must have Registered Nurse license in state in which working and meet one of the following: 

1. Five years clinical experience in the disease specialty of research, or 

2. Bachelor of Science degree with 3 years full time nursing experience or 

3. Certification as a Clinical Research professional

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.

Essential Functions: 

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 for that patient by a licensed physician in the dosage prescribed by protocol.  Retrieval of medication and assessment of compliance by patient to the protocol.

Other Duties: 

Travel for this position is required for protocol and regulatory 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.