Address
Form of workJob Description
Job title:Clinical Trials Nurse Practitioner
Location: Goodyear, AZ
Duration: 0-6 Months (Possibilities of Extension)
Shift:Hours: Monday-Friday 8:30am 7:30pm with 60 min lunch at 1:30pm
Saturday: 9-5:30pm with 30 min lunch at 1 pm
Sunday: 9-4:30pm with 30 min lunch at 1 pm
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 counseling, 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 Principal 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).
- 65 hrs in 2-week period 3 days one week, 4 days the next with every other weekend commitment
- Sample: Week 1: Monday/Tuesday/Friday/Saturday Week 2: Sunday/Wednesday/Thursday
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.
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.
Experience:
- Prior Clinical Trials work experience
- Minimum of two years of medically relevant experience or equivalent
- Effective verbal, written, and electronic communication skills.
- Initiative, problem solving ability, adaptability, and flexibility.
- Ability to work without direct supervision and practice autonomously.
- Is proficient in information management and technology.
- Capacity to collaborate with professional colleagues as necessary to provide quality care.
- Basic Life Support (BLS) certification
- Take and pass a FIT test with the respirators that Client provides and wear the provided respirator mask when protocol requires.
Education:
- Master’s degree level Family Nurse Practitioner program with current National Board Certification and State of Employment license to practice in the Advanced Practice Nurse role required.
