RN Research Nurse

We need to output HTML fragment with sections: h3 headings for sections present. The posting includes: Benefits, Job Summary (maybe "Job Summary" as heading?), Responsibilities (Job Duties), Minimum Requirements (Education, Credentials, Licenses, Specialized Knowledge, Kind And Length Of Experience, FLSA Status). Also maybe "Why You’ll Love Working with St. Elizabeth Healthcare" is a section? Could be "About the role"? Actually there is a paragraph about mission etc. Could be "About the role" or "About us". The instruction: use h3 for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). So we need to map content to those headings if appropriate. We have: - Intro: "Engage with us for your next career opportunity. Right Here. Job Type Regular Scheduled Hours 40 💙 Why You’ll Love Working with St. Elizabeth Healthcare At St. Elizabeth Healthcare, every role supports our mission..." This is like "About the role" or "About us". Could be "About the role". We'll put heading

About the role

and then paragraph(s) containing that content (excluding job type line maybe). The "Job Type Regular Scheduled Hours 40" is metadata; we can fold into a short

or drop. Probably include as a short paragraph:

Job Type: Regular • Scheduled Hours: 40

. But we should not repeat job title as heading. It's fine. - Benefits: There's a "🌟 Benefits That Support You" section with bullet list. So heading

Benefits

then

• ... items. - Job Summary: There's a "Job Summary" paragraph. Could be heading

  Job Summary

  then paragraph. - Responsibilities: There's "Job Description Job Duties:" then a long list of duties. So heading

  Responsibilities

  then
  • each duty. - Minimum Requirements: There's "Minimum Requirements Education, Credentials, Licenses:" then bullet items? Actually it's a paragraph with items separated by line breaks? It lists: Bachelor’s degree in nursing; If eligible, must have a Compact (multi-state) License in their primary state of residence. Then "Specialized Knowledge Ability to effectively manage and prioritize multiple tasks while meeting tight deadlines." Then "Kind And Length Of Experience 2 Years of Nursing Experience". Then "FLSA Status Exempt". So we could group under

    Requirements

    (or Qualifications). Use

    Requirements

    then
    • for each. We should not include Pay or Schedule sections because not specified (though they gave Scheduled Hours 40 but that's not pay). So we omit Pay and Schedule. We must not include boilerplate like EEO etc. There's none. We must preserve all substantive info. Ensure we don't lose any details. Let's extract content precisely. First, the intro lines: "Engage with us for your next career opportunity. Right Here. Job Type Regular Scheduled Hours 40 💙 Why You’ll Love Working with St. Elizabeth Healthcare At St. Elizabeth Healthcare, every role supports our mission to provide comprehensive and compassionate care to the communities we serve. For more than 160 years, St. Elizabeth Healthcare has been a trusted provider of quality care across Kentucky, Indiana, and Ohio. We’re guided by our mission to improve the health of the communities we serve and by our values of excellence, integrity, compassion, and teamwork. Our associates are the heart of everything we do." We need to separate job type line maybe as a short p. The rest is about the organization. We'll produce:

      Job Type: Regular • Scheduled Hours: 40

      Then

      About the role

      with paragraph(s) containing the mission etc. But the instruction: "Do NOT repeat the job title as a heading (the page already shows it) and do NOT put Job ID / requisition numbers as headings — fold minor metadata into a short

      or drop it." So we can put job type line in a p. Now Benefits section: Original: "🌟 Benefits That Support You We invest in you — personally and professionally. Enjoy Competitive pay and comprehensive health coverage within the first 30 days. Generous paid time off and flexible work schedules Retirement savings with employer match Tuition reimbursement and professional development opportunities Wellness, mental health, and recognition programs Career advancement through mentorship and internal mobility" We need to turn into list items. Each sentence seems a benefit. Let's split: - Competitive pay and comprehensive health coverage within the first 30 days. - Generous paid time off and flexible work schedules - Retirement savings with employer match - Tuition reimbursement and professional development opportunities - Wellness, mental health, and recognition programs - Career advancement through mentorship and internal mobility We'll put each as

    • . Job Summary: "Coordinate clinical research studies for the principal investigators and coordinate and promote the research program within St. Elizabeth and the community. Responsible for collaborating with physicians to open studies, educating staff about current studies, educating clients about studies, and obtaining informed consents. Responsibilities include screening and enrolling subjects in studies and managing their participation according to ethical, regulatory, and protocol specific requirements. Responsibilities also include data collection and regulatory compliance. Demonstrate respect, dignity, kindness, and empathy in each encounter with all patients, families, visitors, and other employees regardless of cultural background." We'll put as paragraph(s) under

      Job Summary

      . Responsibilities: The long list after "Job Description Job Duties:" We need to extract each duty as list item. Let's copy the duties text: "Coordinate clinical research studies conducted by the principal investigator. Perform study conduct in accordance with the protocol, manual of operations, and standard operating procedures (SOPs). Collaborate with physicians to open new studies at St. Elizabeth and to promote the research program within the community. Work directly with principal investigator to assist in the design of recruitment strategies, communication plan, and patient safety monitoring plan. Confer with potential study participants to explain the study and obtain the study specific IRB approved informed consent, as well as appropriate HIPAA Authorization before performing any study related procedures. Review with the participant and family all study requirements including diagnostic procedures, questionnaires, and treatments. Conduct participant research visits and collect/record research related data. Submit study data to study sponsors as required and enter in patient’s medical record as appropriate. Maintain the integrity and privacy of participant’s research protocol chart with all required source data. Initiate/coordinate drug orders, laboratory/imaging procedures and treatments for participants based on protocol requirements. Maintain investigational device/product inventory or coordinate investigational device/product accountability with St. Elizabeth pharmacy or appropriate clinical departments. Administer investigational study medication and document in the medical record or coordinate the administration of investigational medication by clinical personnel. Assist with documentation and submission for approvals, revisions, renewals, informed consents, unanticipated problems, and study closure as mandated by the study sponsors, St. Elizabeth Healthcare, and the Institutional Review Board (IRB). Ensure compliance with protocol guidelines and requirements of regulatory agencies, including required documentation and record retention. Monitor patient’s progress and report adverse events/protocol deviations as required. Participate in quality assurance activities of the sponsor, the FDA, the IRB, and other regulatory and accrediting agencies. Performs duties within the scope of the appropriate state Nurse Practice Act and conducts research studies according to the Office for Human Research Protections (OHRP) and US Food and Drug Administration (FDA) regulations and guidelines. Follows Good Clinical Practices, Good Laboratory Practices, St Elizabeth Healthcare policies, and maintains related certifications. Obtains patient biological specimens or works with SEH laboratory / SEH clinical nursing staff to obtain laboratory specimens (blood, urine, saliva, etc.). Maintains IATA certification for the safe handling and shipping of biologic specimens. Works with clinical departments and finance departments to ensure appropriate billing/coding of study related activity. Assists with development of research billing grids, budgets, and monitoring of reimbursements. Performs other duties as assigned." We'll make each line a
    • . Minimum Requirements: Let's extract: "Education, Credentials, Licenses: Bachelor’s degree in nursing If eligible, must have a Compact (multi-state) License in their primary state of residence. Specialized Knowledge Ability to effectively manage and prioritize multiple tasks while meeting tight deadlines. Kind And Length Of Experience 2 Years of Nursing Experience FLSA Status Exempt" We can format as list: - Bachelor’s degree in nursing - If eligible, must have a Compact (multi-state) License in their primary state of residence. - Ability to effectively manage and prioritize multiple tasks while meeting tight deadlines. - 2 Years of Nursing Experience - FLSA Status: Exempt We'll put under

      Requirements

      . We should not include "Pay" or "Schedule" sections. Now produce HTML fragment. We need to ensure proper nesting:

      About the role

      ... mission etc.

      maybe multiple paragraphs. We'll combine the mission paragraph into one

      . Let's craft:

      About the role

      At St. Elizabeth Healthcare, every role supports our mission to provide comprehensive and compassionate care to the communities we serve. For more than 160 years, St. Elizabeth Healthcare has been a trusted provider of quality care across Kentucky, Indiana, and Ohio. We’re guided by our mission to improve the health of the communities we serve and by our values of excellence, integrity, compassion, and teamwork. Our associates are the heart of everything we do.

      Then the job type line:

      Job Type: Regular • Scheduled Hours: 40

      Then Benefits:

      Benefits

      • Competitive pay and comprehensive health coverage within the first 30 days.
      • Generous paid time off and flexible work schedules
      • Retirement savings with employer match
      • Tuition reimbursement and professional development opportunities
      • Wellness, mental health, and recognition programs
      • Career advancement through mentorship and internal mobility
      Job Summary:

      Job Summary

      Coordinate clinical research studies for the principal investigators and coordinate and promote the research program within St. Elizabeth and the community. Responsible for collaborating with physicians to open studies, educating staff about current studies, educating clients about studies, and obtaining informed consents. Responsibilities include screening and enrolling subjects in studies and managing their participation according to ethical, regulatory, and protocol specific requirements. Responsibilities also include data collection and regulatory compliance. Demonstrate respect, dignity, kindness, and empathy in each encounter with all patients, families, visitors, and other employees regardless of cultural background.

      Responsibilities:

      Responsibilities

      • Coordinate clinical research studies conducted by the principal investigator.
      • Perform study conduct in accordance with the protocol, manual of operations, and standard operating procedures (SOPs).
      • Collaborate with physicians to open new studies at St. Elizabeth and to promote the research program within the community.
      • Work directly with principal investigator to assist in the design of recruitment strategies, communication plan, and patient safety monitoring plan.
      • Confer with potential study participants to explain the study and obtain the study specific IRB approved informed consent, as well as appropriate HIPAA Authorization before performing any study related procedures.
      • Review with the participant and family all study requirements including diagnostic procedures, questionnaires, and treatments.
      • Conduct participant research visits and collect/record research related data.
      • Submit study data to study sponsors as required and enter in patient’s medical record as appropriate.
      • Maintain the integrity and privacy of participant’s research protocol chart with all required source data.