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Sub-Investigator, Nurse Practitioner (Np), Clinical Research, Site Management Operations

0-2 years
$95,100 – $237,700*
10 Sept. 10, 2025
Job Description
Job Type: Part Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Description

Position: Nurse Practitioner (APRN, CNP) – Clinical Research
Location: On-site, San Angelo, Texas
Type: Part-Time


Why Join Us?

  • Innovative Environment: Thrive in a setting that encourages creativity and forward-thinking.

  • Passionate Team: Work alongside a group dedicated to making a real difference in healthcare.

  • Cutting-Edge Technology: Access the latest tools and resources advancing medical research.

  • No Prior Research Experience Required: Comprehensive clinical research training will be provided.

Take the leap and apply today to contribute to the future of healthcare!


Key Responsibilities

  • Conduct physical examinations.

  • Assess lab values and evaluate EKGs.

  • Monitor subject compliance with study drug usage and follow-up visits.

  • Evaluate subject response to therapy.

  • Document adverse events and assess their relation to treatment.

  • Provide medical care for treatable adverse events.

  • Communicate with primary care physicians regarding subject participation (as needed).

  • Record study events in subject source documents.

  • Report serious adverse events promptly to the Principal Investigator (PI) and study coordinator.

  • Review and familiarize with investigational products and study-related documents.

  • Ensure effective communication with subjects, research team, IRB, and sponsors.

  • Participate in regular team meetings to discuss subject progress, issues, and protocol processes.

  • Perform other duties as assigned.


Qualifications

  • Valid and current Advanced Practice Registered Nurse (APRN) and Certified Nurse Practitioner (CNP) license in Texas.

  • Strong commitment to ethical research practices and patient safety.

  • Clinical experience in patient care required.

  • Experience with Clinical Trial Management Systems (CTMS) is a plus.

  • IV certification preferred.

  • No history of license suspension or debarment in any state or by the FDA.


About IQVIA

IQVIA is a global leader in clinical research, healthcare intelligence, and commercial insights. We create intelligent connections to accelerate medical innovations, improve patient outcomes, and advance population health worldwide.

Learn more: jobs.iqvia.com


Compensation & Benefits

  • Base Pay Range (Annualized): $95,100 – $237,700*
    *Actual pay will vary based on qualifications, experience, location, and schedule (full-time or part-time).

  • Additional compensation opportunities: incentive plans, bonuses, and other benefits.

  • Comprehensive health, welfare, and employee programs available.


Equal Opportunity Statement

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, protected veteran status, or any other status protected by applicable law.
Learn more here