Clinical Research Registered Nurse

Parameters Research Laboratory, Inc.

Broomfield, COFull-timePosted Jun 12, 2026

Behavioral Health Market Context

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Benefits

Competitive compensation based on experienceHealth, dental, and vision insurancePaid time off and holidaysRetirement plan optionsCompensation $40-50 per hour based on experience

Job Description

Company Description Parameters Research Laboratory, Inc. is dedicated to advancing innovation and excellence in clinical research, with a strong focus on device studies and physiological monitoring, especially blood pressure devices. The team provides a welcoming, professional environment for participants while maintaining the highest standards of safety and care. The organization follows Good Clinical Practice (GCP) guidelines and operates under a robust Quality Management System to ensure regulatory compliance for investigational device trials. Parameters Research Laboratory partners closely with sponsors to design protocols, manage IRB submissions, oversee study conduct, and safeguard data and physical research materials. Comprehensive data management and analysis support sponsors with reliable, actionable study results.

Role Description This full-time, on-site Clinical Research Registered Nurse role is based in Broomfield, CO. The Clinical Research RN will coordinate and conduct clinical research activities for investigational device studies, including participant screening, informed consent, enrollment, and follow-up visits in accordance with study protocols and GCP. Daily responsibilities include performing clinical assessments, collecting and documenting study data, administering study procedures, and monitoring participant safety, including timely reporting of adverse events. The nurse will collaborate with investigators, study coordinators, and sponsors to ensure protocol adherence, visit scheduling, and accurate source documentation and electronic data entry. Additional duties include maintaining study supplies, supporting regulatory and IRB submissions, assisting with monitoring visits and audits, and contributing to continuous quality improvement within the research unit.

Required Qualifications
• Minimum 2 years of experience in Nursing.
• Strong clinical foundation in Nursing and Medicine, with an active, unrestricted Registered Nurse (RN) license in the state of Colorado (or eligibility for licensure).
• Background in Critical Care Nursing or other specialty nursing areas is highly desirable for complex or high-acuity study populations.
• Proficiency in accurate clinical documentation, electronic data capture, and maintaining organized study records.
• Excellent communication and interpersonal skills to work effectively with participants, investigators, sponsors, and the research team.
• Strong attention to detail, critical thinking, and problem-solving skills in a regulated research environment.
• Ability to work on-site full time in Broomfield, CO, 5 days/week, including occasional flexible hours based on study needs.
• Ability to travel based on study needs.

Preferred Qualifications
• Experience in clinical Research and the ability to apply and follow detailed Protocol requirements in accordance with GCP and regulatory standards.
• Current BLS certification; ACLS or other advanced certifications preferred.
• Previous experience in device trials, outpatient clinic settings, or hospital-based research is a plus.

Benefits
• Competitive compensation based on experience.
• Health, dental, and vision insurance.
• Paid time off and holidays.
• Retirement plan options.

Compensation $40-50 per hour based on experience

Qualifications

  • Minimum 2 years of experience in Nursing
  • Strong clinical foundation in Nursing and Medicine, with an active, unrestricted Registered Nurse (RN) license in the state of Colorado (or eligibility for licensure)
  • Proficiency in accurate clinical documentation, electronic data capture, and maintaining organized study records
  • Excellent communication and interpersonal skills to work effectively with participants, investigators, sponsors, and the research team
  • Strong attention to detail, critical thinking, and problem-solving skills in a regulated research environment
  • Ability to work on-site full time in Broomfield, CO, 5 days/week, including occasional flexible hours based on study needs
  • Ability to travel based on study needs

Responsibilities

  • The organization follows Good Clinical Practice (GCP) guidelines and operates under a robust Quality Management System to ensure regulatory compliance for investigational device trials
  • Parameters Research Laboratory partners closely with sponsors to design protocols, manage IRB submissions, oversee study conduct, and safeguard data and physical research materials
  • Comprehensive data management and analysis support sponsors with reliable, actionable study results
  • Role Description This full-time, on-site Clinical Research Registered Nurse role is based in Broomfield, CO
  • The Clinical Research RN will coordinate and conduct clinical research activities for investigational device studies, including participant screening, informed consent, enrollment, and follow-up visits in accordance with study protocols and GCP
  • Daily responsibilities include performing clinical assessments, collecting and documenting study data, administering study procedures, and monitoring participant safety, including timely reporting of adverse events
  • The nurse will collaborate with investigators, study coordinators, and sponsors to ensure protocol adherence, visit scheduling, and accurate source documentation and electronic data entry
  • Additional duties include maintaining study supplies, supporting regulatory and IRB submissions, assisting with monitoring visits and audits, and contributing to continuous quality improvement within the research unit


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