Clinical Trials Nurse Practitioner

Company: Integrated Resources, Inc
Location: Peoria
Posted on: March 19, 2023

Job Description:

Position: Clinical Trials Nurse Practitioner

Location: Peoria, AZ, 85381

Duration: 3-4months



Position Summary:

The Clinical Trials Nurse Practitioner delivers patient care services in a retail clinic environment - all work will be performed in a Client location. You will work in collaboration with a dedicated team of professionals as you independently provide holistic, evidenced-based care inclusive of accurate assessment, diagnosis, treatment, management of health problems, health counselling, and disposition planning for our patients, who are age 18 months and above. Encounters are documented utilizing an electronic health record (EHR). Clinical Trials Nurse Practitioner report directly to the Senior Practice Manager.

Serve as a Sub-Investigator clinician for the clinical trials site, ensuring all elements of clinical trials work are completed in compliance with standard operating procedures. The Sub-Investigator is under the supervision of the Principle Investigator and is responsible for performing study related procedures and /or to make important study-related decisions in compliance with the ethical conduct of the study.

Ability to perform Basic Life Support (BLS) assistance, including but not limited to performing CPR and operating an Automated External Defibrillator (AED).

Duties:

Perform all study responsibilities in compliance with the IRB approved protocol.

Document all findings in subject specific source documents.

Provide ongoing assessment of the study subject/patient to identify Adverse Events

Ensure proper documentation and reporting of all Adverse Events and Serious Adverse Events

Perform physical examinations as part of screening evaluation and active study conduct.

Provide medical management of adverse events as appropriate.

Complete all study documentation in accordance with the study specific requirements.

Communicate with Sponsors and auditors as requested.

Possess a working knowledge of GCP/ICH guidelines, Clinic SOPs, QA/QC procedures, and Investigator 1572 Form.

Review Investigator's Brochure prior to performing any study related activities.

Participate in on-call activities as required to ensure adequate medical coverage.

Monitor safety and well-being of study participants at all times.

Delegate study responsibilities as appropriate to trained study staff.

Educate patients on health maintenance and respond to patient care inquiries.

Document all patient care within an EHR according to company policies and procedures.

Provide care and coordination of our patients with internal and external colleagues, including the broader patient centered medical home, ensuring the highest standard of care is provided for all patients and at all times

Effectively work within a patient care team, including fellow Providers, Collaborative Physicians, paraprofessionals, Pharmacists, and other members of the health care team

The Sub-Investigator/Co-Investigator may also perform all or some of the functions of the Principal Investigator (PI as delegated by the Principal Investigator. The sub-investigator/co-Investigator is under the supervision of the PI and is responsible for performing study related procedures and /or to make important study-related decisions in compliance with the ethical conduct of the study. Responsibilities include but are not limited to:

General study coordination activities

Review participants inclusion and exclusion criteria

Collect medical history.

Physical exam

Collect vitals: body temp, pulse oximetry, respirations, heart rate etc.

Specimen collections and diagnostic assays

Facilitate patient surveys and questionnaires.

Patient education

Patient scheduling

Treatment administration

Liaison with the project management team the PIs clinical research team

Other activities in support of the conduct of the research protocol in accordance with all Federal, State, Local, and Client guidelines.

ADDITIONAL DUTIES

Employee may be required to complete or be responsible for additional job duties as assigned by Primary Investigator, Clinical Trials Operational Lead, Senior Practice Manager, or Area Director.

At the direction of your manager, you may be asked to perform duties outside of the typical day-to-day functions of the role to support various other Client initiatives.

Keywords: Integrated Resources, Inc, Peoria , Clinical Trials Nurse Practitioner, Healthcare , Peoria, Arizona