IQVIA

Nurse Practitioner/Physician Assistant Sub-Investigator, On-Site, Phoenix, AZ

United States · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

  • EmployerIQVIA
  • LocationUnited States
  • Work styleWork style not stated
  • Employment typeFull time
  • Employer posted

Please note this is a fully on site position at the site in Phoenix, AZ.

Are you a Nurse Practitioner or Physicians Assistant ready to embark on an exciting career path in Clinical Research? Avacare is looking for an intellectually curious mid-level provider who thrives in an innovative environment. Join our dynamic team, united by a passion for advancing healthcare and supported by the latest technology.

Why Join Us?

  • Innovative Environment: Thrive in a setting that encourages creativity and forward-thinking.
  • Passionate Team: Be part of a group dedicated to making a difference in healthcare.
  • Cutting-Edge Technology: Work with the latest tools and resources to advance medical research.
  • No Experience in Clinical Research? No Problem! Bring your qualifications, and we will provide comprehensive training in Clinical Research.

Take the leap and apply today to learn more about this unique opportunity to shape the future of healthcare!

Show full description

Responsibilities:

  • Perform Physical Exams
  • Assess Lab Values and Evaluate EKGs
  • Monitor Subject Compliance with study drug use and follow-up visits
  • Evaluate Subject Response to therapy
  • Document Adverse Events and determine their relationship to treatment
  • Provide Medical Care for treatable adverse events
  • Communicate with Primary Care Physicians about subject participation if requested
  • Record Study Events in subject’s source documents
  • Report Serious Adverse Events promptly to the PI and study coordinator
  • Familiarize with Investigational Products and related documents
  • Effective Communication with subjects, research team, IRB, and sponsors
  • Regular Team Meetings to discuss subject participation, issues, and protocol processes
  • Other Duties as Assigned

Qualifications:

  • Must hold a valid and current Advanced Practice Registered Nurse (APRN) and Certified Nurse Practitioner (CNP) license or Physician Assistant License in Arizona
  • Commitment to Ethical Research Practices and patient safety
  • Experience with CTMS a plus
  • No History of License Suspension or debarment in any state or by the FDA
  • Clinical Experience working with patients
  • IV Certification a plus

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $95,100.00 - $237,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Staying safe while you apply

  • Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
  • Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
  • Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

  • Check the fit.

    Compare the requirements with the experience you have confirmed, including gaps.

  • Prepare honestly.

    Build interview stories and application drafts from your own evidence.

  • Keep track.

    Save the role and record your own application status and follow-ups.

Create a free workspace or log in.

At a glance

  • Employment typeFull time
  • Employer posted
  • Added to ROLIVA
  • Last checked

Explore similar roles

Similar jobs