Clinical Research Nurse (will consider non-RN candidate) - Hatton Research Institute

TriHealth•Cincinnati, OH

13d•Onsite

About The Position

Make a difference every day as a Registered Nurse at TriHealth Hatton Research Institute. Join a compassionate, servant-led team committed to excellence in patient care while working in a supportive, high-energy environment. We offer career growth opportunities, and a comprehensive benefits package. Apply today and grow your career with a team that truly values you. Location: Bethesda North Hospital at 10496 Montgomery Road Suite 103 Cincinnati, OH 45242 Work Schedule: Full-Time (80 hours bi-weekly) Day shift No weekends or holidays

Requirements

Bachelor's Degree - Nursing (Required)
2 - 3 years’ experience in Clinical Nursing Critical Thinking (Required)
Proficient in Microsoft Office programs
Knowledge of clinical research
Registered Nurse Upon Hire Required
Basic Life Support (BLS) Upon Hire Required

Responsibilities

Demonstrates the ability to develop processes to facilitate implementation of the research protocol to provide effective and safe medical research to all subjects.
Demonstrates the ability to identify potential and/or actual issues, which may prohibit the accurate implementation of the research protocol and initiate interventions to avoid protocol violations and/or unsafe practice.
Demonstrates the ability to coordinate necessary activities between the Study Coordinators and the Principal Investigator.
Performs initial and ongoing assessments of research subjects and implements care directed towards optimal outcomes.
Plans care for research subjects/families based on assessment, standards of care, optimal outcomes and protocol requirements.
Implements and evaluates plan of care.
Performs technical skills according to policy and procedure and accepts TriHealth Standards.
Documents in medical records appropriately.
Comply with all IRB/FDA requirements in study submissions.
Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment.
Assures compliance with IRB/FDA standards and deadlines in completing Progress Reports.
Assures compliance with IRB/FDA standards and deadlines in reporting all deaths and adverse events within study subjects.
Assures compliance with IRB/FDA standards and deadlines in facilitating communication between study sponsor and designated IRB.
Appropriately and accurately assesses potential subjects for inclusion and exclusion criteria.
Keeps Case Report Forms complete and thorough using the IRB and FDA standards.
Supports hospital staff in complying with research protocols and works to minimize the impact on their workload.
Keeps queries and protocol violations that can be controlled to a minimum.
Responds appropriately and accurately to all queries in a timely fashion.
Demonstrates knowledge of available studies, screening potential patients for eligibility, guiding physicians and staff in needed timetables for appropriate randomization.
Participates in the identification and selection of good clinical protocols based on subject selection, safe medical practice and resource availability.
Attends training required by sponsoring organizations for specific protocols and/or attends meetings related to the initiation or on-going progress of a sponsored clinical trial.
Acts as the point person for audit staff coming into institution for a review prepares a written response with a plan of action to any major/minor deficiencies.