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IQVIA

Nurse Practitioner/Physician Assistant – Sub-Investigator

IQVIA

Nurse Practitioner/Physician Assistant conducting medical responsibilities in Clinical Research. Emphasis on patient care, compliance, and team collaboration using advanced medical technologies.

Posted 7/12/2026full-timePhoenix • Arizona • 🇺🇸 United StatesMid-LevelSenior💰 $95,100 - $237,700 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in conducting physical exams, evaluating lab values, and monitoring patient compliance in clinical research settings. Proficient in documenting adverse events and communicating effectively with healthcare teams and subjects.

Highest-signal resume keywords
Advanced Practice Registered Nurse (APRN) LicenseCertified Nurse Practitioner (CNP) LicenseClinical ExperienceEthical Research PracticesIV Certification

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Physical ExamsLab Value AssessmentEKG EvaluationAdverse Event DocumentationPatient Monitoring
Soft Skills
Effective CommunicationTeam Collaboration
Tools & Technologies
CTMS
Certifications & Qualifications
Advanced Practice Registered Nurse (APRN)Certified Nurse Practitioner (CNP)IV Certification
Industry Keywords
Investigational ProductsPatient SafetyEthical Research PracticesSerious Adverse EventsIRB

About the role

Key responsibilities & impact
  • 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

Requirements

What you’ll need
  • Must hold a valid and current Advanced Practice Registered Nurse (APRN) and Certified Nurse Practitioner (CNP) license in Texas.
  • 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

Benefits

Comp & perks
  • Cutting-Edge Technology
  • Comprehensive training in Clinical Research
  • Passionate Team
  • Innovative Environment