Clinical Research Nurse Practitioner - Sub Investigator

Updated 10/14/25
80501, Longmont, Colorado, United States
Nurse Practitioner
Family Practice/Primary Care
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Job at a glance

Degree Required MSN/MSRN
Position Type Full-Time
Work Environment Clinic/Private Practice Outpatient
Visa Sponsorship No
Experience Level 2 years

Job description

Job description Job Title: Clinical Research Nurse Practitioner - Sub-Investigator
Location: Longmont, CO (35 miles north of Denver, CO)
Position Type: Full-Time, Permanent Placement

About the Role

We are seeking a skilled and motivated Clinical Research Nurse Practitioner to join our research team in Longmont, CO. The NP will serve as a Sub-Investigator on clinical trials, working closely with the Medical Director and clinical research staff to ensure the safe and effective execution of protocols. This is a full-time, permanent opportunity for an NP with experience in clinical research who is passionate about advancing medical innovation while providing high-quality patient care.

Key Responsibilities

  • Serve as a Sub-Investigator (Sub-I) on clinical trials under the supervision of the Principal Investigator/Medical Director.
  • Perform delegated medical assessments and procedures in strict accordance with study protocols.
  • Conduct and document study-related assessments, including physical exams, medical history reviews, and safety evaluations.
  • Collaborate with study coordinators and other research staff to ensure protocol compliance, accurate data collection, and patient safety.
  • Evaluate and manage adverse events, ensuring proper reporting and follow-up per regulatory and sponsor requirements.
  • Maintain current knowledge of study protocols, informed consent processes, and GCP/ICH guidelines.
  • Participate in study initiation, monitoring, and close-out visits as required.
  • Perform additional duties as delegated by the Medical Director.

Qualifications

  • Nurse Practitioner (NP) licensure in the state of Colorado (active and unrestricted).
  • Minimum 1 year of full-time clinical research experience (required).
  • Experience as a Sub-Investigator or in direct clinical trial involvement preferred.
  • Strong knowledge of GCP, ICH guidelines, and FDA regulations.
  • Excellent clinical judgment and ability to make sound medical decisions within scope of practice.
  • Strong organizational, communication, and interpersonal skills with the ability to work collaboratively in a multidisciplinary research environment.

Compensation & Benefits

  • Competitive salary (commensurate with experience).
  • Full-time, permanent placement with benefits (details provided upon discussion).
  • Opportunity to work with an experienced research team advancing innovative therapies.

Working Hours

Monday - Friday: 8 AM - 5 PM
By applying you agree to our Terms of Service

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Medix
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Job Description

Explore the area

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Hiring Organization

Medix
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