RN Research Clinical Trials
3 days ago
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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