RN Research Clinical Trials

2 weeks ago

dallas, United States Baylor Scott & White Health Full time

Job Title: Research RN 1

Location: Dallas, TX

Facility: BSWH-Baylor University Medical Center

Department: Baylor Research Institute

Shift/Status: Full-Time, 40 hours/week, Monday - Friday, 8:00-5:00 PM 

**This position will be on-site. Department looking for previous Research and clinical trial experience. **

JOB SUMMARY

Baylor Scott & White Health is looking for an experienced RN to work with our research team in the Dallas area.  This unique position will allow the selected individuals to cross train and work on studies in Infectious Disease, GI, Kidney, Interventional Radiology and Neuro.  Experience in Research is preferred.  Experience in a hospital or clinic setting is required.  

About Us

At Baylor Scott & White Health, we prioritize the well-being of people, families, and communities. It is the largest non-profit healthcare system in Texas that focuses on empowering healthy lifestyles.

Our Core Values are:

  • We serve faithfully by doing what's right with a joyful heart.
  • We never settle by constantly striving for better.
  • We are in it together by supporting one another and those we serve.
  • We make an impact by taking initiative and delivering exceptional experience.

Benefits

Our competitive benefits package empowers you to live well and provides:

  • Eligibility on day 1 for all benefits
  • Dollar-for-dollar 401(k) match, up to 5%
  • Debt-free tuition assistance, offering access
    to many no-cost and low-cost degrees, certificates and more
  • Immediate access to time off benefits

At Baylor Scott & White Health, your well-being is our top priority. 

Note: Benefits may vary based on position type and/or level

Job Summary

As a Research Nurse 1, you'll assist principal investigators with clinical trials following guidelines. Gain knowledge on trial phases from start to finish. Learn all aspects of the position.

What You'll Do

  • Collaborating with departments on research. Working under a research head. Interacting with investigators and managers. Provide education for healthcare professionals. Coordinate with Pharmacy for projects.
  • You will learn to review new study protocols and materials from sponsors.
  • You will screen patients for clinical trial eligibility according to HIPAA standards, which is a core part of your role.
  • You'll help complete study activities by returning supplies, disposing unused stock, and addressing all queries thoroughly.
  • Your responsibilities will also extend to assisting with the preparation of final reports for the Institutional Review Board.
  • You'll develop skills to effectively use the Study Assistant Clinical Trials Management System, as per departmental requirements.

What Will Make You Successful In The Role

  • Outstanding ability in both written and spoken communication.
  • Highly developed computer skills, including proficiency in Microsoft Office suite particularly Excel and PowerPoint.
  • Proven capability to handle time-sensitive projects while adhering to strict deadlines.
  • Best skills in establishing and maintaining productive working relationships.
  • Past experience of less than a year is acceptable, though not mandatory.

Belonging Statement

We think everyone should feel welcomed, valued, and supported. Our workforce should mirror our communities.

Qualifications

  • Associate's degree.
  • Registered Nurse (RN) License.
  • BLS certification within 30 days.

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