Clinical Research Nurse Practitioner - Sub Investigator

Medix

Longmont, COFull-timePosted Mar 29, 2026

Behavioral Health Market Context

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Benefits

Health Insurance

Job Description

ctor 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

Qualifications

  • Nurse Practitioner (NP) licensure in the state of Colorado (active and unrestricted)
  • Minimum 1 year of full-time clinical research experience (required)
  • 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

Benefits

  • 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

Responsibilities

  • 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
  • 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
  • Working Hours: Monday - Friday: 8 AM - 5 PM


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