RN - Clinical Research Float - FT

Guthrie; Sayre (Bradford County); On-site; USD 55,000 - 75,000; Full time

Job summary

Guthrie in Sayre, PA, is seeking an RN - Clinical Research Float to coordinate multiple clinical research protocols across in-patient and out-patient settings. The role requires deep knowledge of disease pathophysiology, pharmacology, patient evaluation workflows, and the ability to communicate new research processes with involved departments.

Candidates must be licensed in PA and NY, with dual licensure within 3 months.

Qualifications

• Must be licensed in PA and NY; dual licensure within 3 months of hire.
• Five years clinical healthcare experience or BSN with 3 years nursing experience or CRP certification.
• Three years full-time nursing experience required.

Responsibilities

• Coordinate multiple clinical research projects across disease conditions.
• Meet sponsor training requirements and train team members accordingly.
• Support regulatory specialists with sponsor communications and IRB activities.
• Maintain study supply inventory and assist monitors during visits.
• Develop and advance department research program plans with leadership.
• Schedule patient visits, educate on study requirements, and document encounters.
• Administer investigational medications ordered by licensed physicians.
• Travel between Guthrie research sites as required.

Skills

Clinical research coordination

Regulatory documentation

Sponsor communications

Patient education

Project coordination

Education

Bachelor of Science degree with 3 years nursing experience

Clinical Research Professional Certification

PA and NY RN licensure

Job description

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!

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

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.

"Must have a Registered Nursing license in PA and NY** and meet one of the following:"

1. Five years clinical experience in a healthcare setting, 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.
• 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

• 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.