Baylor College of Medicine
Summary
This Research Nurse position is within the Office of Clinical Research (OCR), which provides centralized support to investigators who conduct studies at Baylor College of Medicine and affiliated hospitals. The role requires responsible patient care in a clinical research setting, including obtaining vital signs, performing ECGs, starting IV lines, collecting and processing specimens, administering medications, and monitoring patients. Duties also include maintaining accurate records, ensuring protocol compliance, and performing additional procedures as required per protocol. The candidate may need to work after‑hours, weekends, and overnight, and must be able to travel between Baylor College of Medicine and affiliated hospitals within the Houston Texas Medical Center.
Job Duties
Assist the Clinical Research Manager with pre‑study visits and feasibility assessments.
Coordinate and ensure accurate protocol implementation for all assigned protocols.
Adhere to the scope of practice as defined by the Texas Nurse Practice Act.
Collect study specimens and check subjects’ vital signs.
Administer study medications.
Follow subjects’ progress and advise the Principal Investigator.
Maintain patient charts and medical records.
Ensure the clinical studies are conducted in accordance with FDA and other regulatory guidelines.
Educate patients on significant aspects of the study.
Serve as a liaison and distribute research information to faculty, research staff, principal investigator, and others as required.
Maintain a clean and safe work environment.
Stock and order study supplies.
Provide training and guidance to research nurses and other research personnel, serving as a resource to staff.
Travel between study site locations as needed.
Work flexible hours and independently with minimal supervision.
Perform other job‑related duties as assigned.
Minimum Qualifications
Associate’s or Bachelor’s Degree in Nursing.
Four years of relevant experience as a licensed Registered Nurse (RN), with at least one year in research nursing. Degrees in lieu of experience will not be accepted.
Current RN license issued by the State of Texas Board of Nursing and Basic Life Support (BLS) certification.
Preferred Qualifications
Experience supporting Phase 1 oncology trials.
Perform PK sampling and processing per protocol.
Monitor patients during long, complex infusions and manage reactions.
Manage adverse events in compliance with GCP and SOPs.
Collaborate with investigators, coordinators, pharmacy, and lab staff.
Oncology and research certifications preferred; detail‑oriented care essential.
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Job Duties
Assist the Clinical Research Manager with pre‑study visits and feasibility assessments.
Coordinate and ensure accurate protocol implementation for all assigned protocols.
Adhere to the scope of practice as defined by the Texas Nurse Practice Act.
Collect study specimens and check subjects’ vital signs.
Administer study medications.
Follow subjects’ progress and advise the Principal Investigator.
Maintain patient charts and medical records.
Ensure the clinical studies are conducted in accordance with FDA and other regulatory guidelines.
Educate patients on significant aspects of the study.
Serve as a liaison and distribute research information to faculty, research staff, principal investigator, and others as required.
Maintain a clean and safe work environment.
Stock and order study supplies.
Provide training and guidance to research nurses and other research personnel, serving as a resource to staff.
Travel between study site locations as needed.
Work flexible hours and independently with minimal supervision.
Perform other job‑related duties as assigned.
Minimum Qualifications
Associate’s or Bachelor’s Degree in Nursing.
Four years of relevant experience as a licensed Registered Nurse (RN), with at least one year in research nursing. Degrees in lieu of experience will not be accepted.
Current RN license issued by the State of Texas Board of Nursing and Basic Life Support (BLS) certification.
Preferred Qualifications
Experience supporting Phase 1 oncology trials.
Perform PK sampling and processing per protocol.
Monitor patients during long, complex infusions and manage reactions.
Manage adverse events in compliance with GCP and SOPs.
Collaborate with investigators, coordinators, pharmacy, and lab staff.
Oncology and research certifications preferred; detail‑oriented care essential.
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