Clinical Research Nurse II: Protocols, Recruitment & Data

UT Health San Antonio; San Antonio (TX); In loco; USD 70.000 - 100.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical insurance

Dental insurance

Vision insurance

Disability insurance

FSAs

Retirement plan

Paid time off

Holidays

Descrizione del lavoro

UT Health San Antonio is seeking a CTO Clinical Research Nurse - Intermediate (MCC) to actively facilitate clinical research by administering and monitoring treatment protocols. You will screen, recruit, consent participants and coordinate study visits within a dynamic research environment.

The role requires a Bachelor of Nursing and at least three years of nursing experience in the designated study area, with the ability to liaise with research teams and stakeholders while ensuring compliance

Competenze

• Bachelor of Nursing required.
• Ability to liaise with participants, research team and stakeholders.
• Experience coordinating multi-participant studies.

Mansioni

• Screens, recruits and consents study participants.
• Verifies eligibility, completes screening procedures, schedules and conducts study visits, collects and processes data.
• Instructs and counsels patients in research procedures, including administration, monitoring and data analysis.
• Ensures compliance with federal and local regulations.
• Monitors study close-out and retains records for required time.
• Reviews protocol goals, plans source documentation, and coordinates study initiation.
• Coordinates and manages clinical research projects for the Principal Investigator.
• Performs other duties as assigned.

Conoscenze

Nursing experience

Formazione

Bachelor's degree in Nursing

Descrizione del lavoro

UT Health San Antonio is seeking a CTO Clinical Research Nurse - Intermediate (MCC) to actively facilitate clinical research by administering and monitoring treatment protocols. You will screen, recruit, consent participants and coordinate study visits within a dynamic research environment.

The role requires a Bachelor of Nursing and at least three years of nursing experience in the designated study area, with the ability to liaise with research teams and stakeholders while ensuring compliance