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
Click
here to apply!
|