Research Nurse - Neurology (Stroke Institute)

UTHealth Houston•Houston, TX

9d•Onsite

About The Position

The mission of the Institute for Stroke and Cerebrovascular Diseases is to advance and transform stroke prevention, treatment, and rehabilitation in the dual contexts of community population health and a learning health-care system. We are committed to high-quality, rigorous research across the continuum of stroke care; developing new treatments and innovative healthcare delivery models for stroke; and promoting stroke awareness and education for the general public. We are a multidisciplinary hub of cutting-edge research dedicated to cerebrovascular, brain, and mental health while providing a valuable resource for patients seeking to participate in groundbreaking research studies. The primary purpose of this position is to support complex clinical trials led by the Institute for Stroke and Cerebrovascular Diseases. This role provides regulatory oversight to ensure study compliance with applicable requirements and serves as a subject matter expert, guiding and educating research teams on the proper execution of clinical trials in accordance with regulatory and institutional standards. Extensive experience in clinical trial research, regulatory and compliance is preferred. What we do here changes the world. UTHealth Houston is Texas’ resource for healthcare education, innovation, scientific discovery, and excellence in patient care. That’s where you come in.

Requirements

Bachelor's Degree in nursing from an accredited nursing school required
1 year of experience in research required
Clinical knowledge
Ethics and Regulations
Interpersonal Skills
Data Management
Health Services\RN - Registered Nurse - State Licensure and/or Compact State Licensure required
Employees must permanently reside and work in the State of Texas.

Nice To Haves

Extensive experience in clinical trial research, regulatory and compliance is preferred.
Research & Development\Association of Clinical Research Professionals - (ACRP-CP) preferred
May substitute required education with equivalent years of experience beyond the minimum experience requirement.

Responsibilities

Recruits, screens & consents participants, and educates research participants regarding the overall research objectives and potential benefits and/or risks for participants, as necessary for research projects.
Coordinates and administers the nursing care functions within a research project in accordance with research protocols and the daily administration and staff supervision of the project.
Schedules follow-up visits and maintains contact with participants, participants' families, department staff, pharmaceutical company representatives, other faculty members.
Distributes research information to faculty, research staff, principal investigator, and others as requested.
Responsible for preparation of regulatory submission to IRB and applicable regulatory agencies as well as the day-to-day activities of enrolling in clinical studies including trials.
Inputs data and maintains research databases and related records needed for research.
Performs other duties as assigned.

Benefits

100% paid medical premiums for our full-time employees
Generous time off (holidays, preventative leave day, both vacation and sick time – all of which equates to around 37-38 days per year)
The longer you stay, the more vacation you’ll accrue!
Longevity Pay (Monthly payments after two years of service)
Awesome retirement/pension plan
Free financial and legal counseling
Free mental health counseling services
Gym membership discounts and access to wellness programs
Other employee discounts including entertainment, car rentals, cell phones, etc.
Resources for child and elder care