Clinical Research Nurse Associate: Study Coordination & Patient Care

UT Health San Antonio

San Antonio (TX)

In loco

USD 65.000 - 85.000

Tempo pieno

42 ore fa
Candidati tra i primi

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Descrizione del lavoro

UT Health San Antonio's Mays Cancer Center is seeking a Clinical Research Nurse-Associate to coordinate and participate in clinical research studies under the supervision of the principal investigator. The role includes recruiting participants, collecting data, ensuring protocol compliance, and supporting study visits to safeguard patient well-being.

The position requires an Associate’s degree, 1 year of nursing experience in the designated study area, and an active Texas RN license with CPR/BLS

Competenze

  • 1 year nursing experience in the designated study area is required.
  • Active Texas RN license is required.
  • Active CPR/BLS required.

Mansioni

  • Screens, recruits and consents study participants.
  • Verifies eligibility, completes screening procedures, schedules and conducts study visits, collects and processes data collection, completes research related forms, completes electronic data entry and maintains study subject data.
  • Instructs and counsels patients in research procedures, to include administration, monitoring, recording and analyzing data.
  • Ensures compliance with all federal and local regulations.
  • Monitors close-out of studies and ensures records are retained for appropriate length of time.
  • Reviews goals and requirements of any new protocols; plans and designs source documentation for protocol; and coordinates study initiation.
  • Coordinates and manages clinical research projects for Principal Investigator via study protocol including assessment, planning, evaluation and intervention for the well-being of study participants.
  • Performs all other duties as assigned.

Conoscenze

Nursing experience

Formazione

Associate’s degree

Descrizione del lavoro

UT Health San Antonio's Mays Cancer Center is seeking a Clinical Research Nurse-Associate to coordinate and participate in clinical research studies under the supervision of the principal investigator. The role includes recruiting participants, collecting data, ensuring protocol compliance, and supporting study visits to safeguard patient well-being.

The position requires an Associate’s degree, 1 year of nursing experience in the designated study area, and an active Texas RN license with CPR/BLS

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