Research RN 1
Behavioral Health Market Context
Benefits
Benefits Our benefits are designed to help you live well no matter where you are on your journeyFor full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include: Immediate eligibility for health and welfare benefits 401(k) savings plan with dollar-for-dollar match up to 5% Tuition Reimbursement PTO accrual beginning Day 1 Note: Benefits may vary based upon position type and/or level
Job Description
About Us Here at Baylor Scott & White Health we promote the well-being of all individuals, families, and communities. Baylor Scott and White is the largest not-for-profit healthcare system in Texas that empowers you to live well. 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 benefits are designed to help you live well no matter where you are on your journey. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include: Immediate eligibility for health and welfare benefits 401(k) savings plan with dollar-for-dollar match up to 5% Tuition Reimbursement PTO accrual beginning Day 1 Note: Benefits may vary based upon position type and/or level. Job Summary Onsite. Monday-Friday; 8a-5p. 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. Essential Functions Of The Role 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. Key Success Factors 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 believe that all people should feel welcomed, valued and supported. Qualifications Associate's degree. Registered Nurse (RN) License. BLS certification within 30 days.
Qualifications
- •Working under a research head
- •Key Success Factors 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
- •Qualifications Associate's degree
- •Registered Nurse (RN) License
- •BLS certification within 30 days
Responsibilities
- •Monday-Friday; 8a-5p
- •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
- •Essential Functions Of The Role Collaborating with departments on research
- •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
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