Senior Research Nurse: Trials & Protocol Coordination

• Registered Nurse plus five years of professional nursing experience in direct patient care or research in approved specialty area.
• Licensed by the State of Texas to practice as a Registered Nurse.
  

Minimum Qualifications:

• Registered Nurse plus five years of professional nursing experience in direct patient care or research in approved specialty area.
• Licensed by the State of Texas to practice as a Registered Nurse.
  

Job Description:
Coordinates and provides advanced professional nursing skills on complex research projects in a unit, clinic, or hospital involving patient related research efforts. Responsibilities include assessing, developing, implementing and evaluation a plan of nursing care in a research unit using advanced professional nursing skills requiring specialized training or experience.
Job Duties:

• Coordinates complex research projects that involve the supervision of research activities.
• Screens patients for protocol eligibility and participation in clinical trials.
• Participates in the coordination and monitoring of patient treatment and dispensing of study medication.
• Monitors and evaluates patient response to protocol treatment in collaboration with the physician.
• Works closely with PI, other healthcare professionals, and potential families of subjects to insure the standards of good clinical practice, IRB requirements, and state-federal regulations are being observed.
• Participates in decision making of research practice, in study design, IRB protocol submission and maintenance.
• Performs chart reviews and analyzes data when authorized by Investigators following HIPAA guidelines.
• Enters and maintains data into database.
• Assists in preparing and entering IRB protocols and proposals and monitors compliance of human subjects.
• Educates patients and assists in obtaining informed consent.
• Schedules study visits and meetings related to studies.
• Maintains education on trials and updates Investigators.
• Performs procedures related to study requirements.
• May perform the following:
• Prepare regulatory documents to be sent to the Sponsor; under direction of PI may draft various communications with Sponsor
• Assist the physician in protocol analysis, using computer statistical/data management packages or present data from clinical trials in publication and/or formal oral presentations.
• Collaborate with the physician and/or protocol sponsor regarding protocol design, implementation and evaluation.
• Provides training and guidance to research nurses and other research personnel and serves as a resource to staff.
• Plans and participates in orientation, peer review and staff development programs.
  

Marginal or Periodic Job Functions:

• Performs related duties as required.
  

Equipment:
Competent use of equipment and related supplies; and use of mechanical devices for healthcare monitoring of the patient subject.
Working Environment/Location of Position:

• Work environment is located in a comfortable indoor area.
• Conditions such as noise, odors, cramped work space and/or fumes could sometimes cause discomfort.
• Moderate to extreme physical effort may be required such as walking, standing and lifting materials, equipment, objects, and/or patients.
• Occasional lifting may be heavy and awkward, over 50 lbs.
• Vision, hearing, talking, and sense of touch abilities must be adequate to enable one to quickly and accurately perform tasks such as: reading small print, reading from monitoring equipment, defining details, sending and receiving clear and accurate verbal communication.
• Frequent periods of concentrated or focused attention will be needed to interpret visual, auditory, and sensory inputs.
• Alternate shift work and/or on call status may be required.
• Alertness and careful attention to detail will be required to avoid injury.
• May be exposed to such occupational hazards as communicable diseases, radiation, chemotherapeutic agents, and disoriented or combative patients.
  

OTHER:

• Attends and participates in campus coordinator workshops
• Prepares for certification exam after requirements are met
• Maintains licensures through continuing education (CEU)
• Basic PC skills, including word processing, report writing & e-mail skills
• Spanish language skills may be a plus
• Good written and verbal English skills
• Developing good organizational and time management skills
  

Salary Range:
Commensurate with experience
Equal Employment Opportunity
UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a Federal Contractor, UTMB Health takes affirmative action to hire and advance protected veterans and individuals with disabilities.
Primary Location
United States-Texas-Galveston
Work Locations
0342 - Research Building 6
Job
Research Academic & ClinicalRegular
Shift
Standard
Employee Status
Non-Manager
Job Level
Day Shift
Job Posting
Jun 24, 2026, 7:42:53 PM #J-18808-Ljbffr