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

Iqvia
IQVIA
2+ years
$95,100 – $237,700 USD
10 Aug. 30, 2025
Job Description
Job Type: Full Time Education: Current and valid Advanced Practice Registered Nurse (APRN) license in Texas. Certified Family Nurse Practitioner (CNP) in Texas. 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 Title:

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


Location:

📍 San Angelo, Texas (Office-Based)
Job ID: R1494924
Job Type: Full-Time (Part-Time Options Available – Minimum 24 hours/week)
Work Arrangement: Fully On-Site


About the Role:

Are you a Nurse Practitioner (FNP) looking to break into clinical research? Avacare, in partnership with IQVIA, is seeking a dedicated and curious mid-level provider to support clinical trial operations. No prior research experience? No problem — comprehensive training will be provided.

Join a passionate, innovative, and tech-driven team advancing the future of healthcare through cutting-edge clinical trials.


Why Join Us?

  • 💡 Innovative Environment – Encourage creativity and new ideas.

  • 🤝 Passionate Team – Work with professionals driven to improve healthcare.

  • 🖥️ Advanced Technology – Use the latest research tools and systems.

  • 🎓 On-the-Job Training – No clinical research experience required.


Key Responsibilities:

  • Perform physical examinations on study participants.

  • Review and assess laboratory values and EKG results.

  • Monitor subject adherence to investigational product use and scheduled visits.

  • Evaluate subject response to study treatments.

  • Identify and document adverse events; assess relationship to study drug.

  • Provide medical care for manageable adverse events.

  • Communicate with participants’ primary care providers when needed.

  • Accurately document clinical and study-related events in source records.

  • Promptly report Serious Adverse Events (SAEs) to PI and study coordinator.

  • Gain familiarity with Investigational Products and associated documentation.

  • Maintain effective communication with:

    • Study participants

    • Internal research team

    • IRBs (Institutional Review Boards)

    • Study sponsors

  • Participate in regular team meetings to review study progress and issues.

  • Perform other research-related duties as assigned.


Qualifications:

Required:

  • Current and valid Advanced Practice Registered Nurse (APRN) license in Texas.

  • Certified Family Nurse Practitioner (CNP) in Texas.

  • Commitment to ethical conduct in clinical research.

  • Clinical experience in patient care.

Preferred:

  • Experience with Clinical Trial Management Systems (CTMS).

  • IV certification.

  • No prior license suspensions or FDA debarments.


Compensation & Benefits:

  • Annual Base Salary Range:
    💵 $95,100 – $237,700 USD
    (Final offer dependent on experience, qualifications, and location)

  • Additional Benefits May Include:

    • Incentive plans

    • Performance bonuses

    • Comprehensive health and welfare benefits


About IQVIA:

IQVIA is a global leader in clinical research and healthcare analytics. We partner with top life sciences companies to accelerate the development of innovative treatments, improve patient outcomes, and transform global health.

🔗 Visit IQVIA Careers


Equal Opportunity Statement:

IQVIA is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

🔗 Equal Employment Opportunity Policy


How to Apply:

Apply now online:
🔗 Apply Now
Job ID: R1494924