Advanced Practice Nurse - FT - Days - Research - Rio Grande City

Advanced Practice Nurse - FT
- Days
- Research
- Rio Grande City - 19365

US:

TX:

Edinburg | Research | Full Time

Posted 2 weeks ago

DHR Health - US:

TX:

Edinburg
- Days

MISSION STATEMENT:

Our Mission is to improve the well-being of those we serve with a commitment to excellence: every patient, every encounter, every time.

VISION:

Our Vision is to create a world-class health system to advance medicine and increase access for the communities we serve by empowering caregivers to heal through compassion, knowledge, innovation, integrated care and excellence.

The Clinical Research APRN will support all human subject clinical trials as a Co-Investigator. This support will entail provision of expert nursing consultation and trial oversight, execution of all clinically-relevant clinical trial activities and procedures with patient safety at the forefront. The Research APRN will facilitate fluid communication with external clinical trial sponsors and contract research organization representatives. The Research APRN will work closely with clinical research study coordinators and all clinical research staff to help expedite successful completion of all human subject clinical trials.

• Graduate of an accredited school for professional nursing MSN required. Successful completion of practitioner program.
• Registered Nurse (RN) and Texas Advanced Practice Registered Nurse license.
• Two (2) years’ experience as nurse practitioner with acute care experience preferred
• Bilingual – English/Spanish.
• Completion of required Human Subject Research Protection Modules provided by the Collaborative Institutional Training Initiative (CITI) and all Good Clinical Practice (GCP) training requirements (Preferred)
• ACLS required within 6 months of hire date
• Excellent customer service skills with emphasis on cultural sensitivity
• Computer skills required with vast knowledge of Microsoft Office suite.
• Excellent written and verbal communication skills required.
• Understands concepts of human subject research and is able to participate in and coordinate research programs in compliance with all codes of federal regulations (45 CFR 46 | HHS.gov)

• Promotes the facility mission, vision and values by effectively communicating them to others. Considers mission, vision and values in developing services, standards and practices
• Primarily responsible to assess, evaluate and treat patients on clinical trials as per clinical trial specificities under the supervision and collaboration of a physician investigator, by using advanced knowledge and skill to identify abnormal conditions, diagnose health problems, develop and implement treatment plans, evaluate patient outcomes, and collaborate with or refer to a physician in the medical practice for further care management.
• Collaborate with designated physician investigators and research team members (consisting of principal investigators, clinical research nurses, clinical research coordinators and clinical research assistants).
• Clinical responsibilities include conducting a history and physical exam, monitoring toxicities, assessing clinical responses and providing exemplary patient care while ensuring the protocol is conducted in a high quality manner. Monitoring toxicities, assessing clinical status and providing direct patient care while insuring the protocol is conducted in a high quality fashion.
• Clinical responsibilities include being available during protocol directed therapy (i.e. infusions, injections, etc) as indicated or necessary depending on the circumstance.
• Clinical responsibilities include management of phone calls/ messages from enrolled clinical trial patients, and working closely with the PI, MD, and nurses to deliver exceptional care.
• Work in collaboration with clinical trial unit managers with initiating study procedures for new Investigator Initiated Trials (IITs) and industry-sponsored clinical trials. Manage all aspects of Phase I – IV clinical trials.
• Participate in the conduct of audits by study sponsors, CROs, the FDA, and other groups.
• Develop and maintain ongoing communication with the clinical teams including,…