Registered Nurse – Clinical Research Team

Confidential

Santa Fe, NMPart-timePosted Mar 9, 2026

30–35 an hour

Behavioral Health Market Context

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Job Description

 setting.

This is a rewarding opportunity for an RN who wants to apply their clinical expertise in a dynamic research environment while making a meaningful contribution to the advancement of medical treatments and patient outcomes.

Key Responsibilities

Patient Care & Study Procedures
• Perform study-related clinical procedures including blood draws, vital signs, ECGs, IV insertions, and specimen collection and processing
• Administer investigational products and study interventions per protocol, under the direction of the Principal Investigator
• Monitor participants during and after study procedures, recognizing and responding to adverse events or safety concerns
• Provide compassionate, patient-centered care and education to research participants throughout their study participation

Research Coordination Support
• Assist with participant screening, eligibility assessments, and informed consent processes
• Accurately document all clinical activities in source documents, electronic data capture (EDC) systems, and case report forms (CRFs)
• Collaborate with research coordinators to ensure protocol adherence and timely completion of study visit activities
• Communicate study updates, protocol requirements, and participant status to the research team

Compliance & Safety
• Maintain compliance with ICH E6(R2) Good Clinical Practice (GCP), FDA regulations, and institutional policies
• Participate in study initiation meetings, protocol training, and ongoing sponsor communications
• Support preparation for regulatory inspections and internal quality audits
• Report adverse events and protocol deviations promptly and accurately per study requirements

Qualifications

Required
• Active, unrestricted Registered Nurse (RN) license in the state of New Mexico
• Minimum 2 years of clinical nursing experience (hospital, ambulatory, or specialty care)
• BLS/CPR certification (ACLS preferred)
• Strong phlebotomy and IV skills
• Excellent documentation habits and high attention to detail
• Ability to work independently and as part of a multidisciplinary team

Preferred
• Prior clinical research or clinical trial experience
• CCRP (Certified Clinical Research Professional) or SoCRA certification, or willingness to obtain
• Familiarity with GCP guidelines and ICH E6 standards
• Experience with electronic data capture (EDC) systems such as REDCap, Medidata Rave, or similar
• Bilingual (English/Spanish) a plus given our Santa Fe patient population

Pay: $30.00 - $35.00 per hour

Work Location: In person

Qualifications

  • Active, unrestricted Registered Nurse (RN) license in the state of New Mexico
  • Minimum 2 years of clinical nursing experience (hospital, ambulatory, or specialty care)
  • Strong phlebotomy and IV skills
  • Excellent documentation habits and high attention to detail
  • Ability to work independently and as part of a multidisciplinary team

Benefits

  • Pay: $30.00 - $35.00 per hour

Responsibilities

  • In this role, you will support the safe and ethical conduct of clinical trials and research studies, working closely with investigators, coordinators, and study sponsors to deliver high-quality patient care within a research setting
  • This is a rewarding opportunity for an RN who wants to apply their clinical expertise in a dynamic research environment while making a meaningful contribution to the advancement of medical treatments and patient outcomes
  • Patient Care & Study Procedures
  • Perform study-related clinical procedures including blood draws, vital signs, ECGs, IV insertions, and specimen collection and processing
  • Administer investigational products and study interventions per protocol, under the direction of the Principal Investigator
  • Monitor participants during and after study procedures, recognizing and responding to adverse events or safety concerns
  • Provide compassionate, patient-centered care and education to research participants throughout their study participation
  • Research Coordination Support
  • Assist with participant screening, eligibility assessments, and informed consent processes
  • Accurately document all clinical activities in source documents, electronic data capture (EDC) systems, and case report forms (CRFs)
  • Collaborate with research coordinators to ensure protocol adherence and timely completion of study visit activities
  • Communicate study updates, protocol requirements, and participant status to the research team
  • Compliance & Safety
  • Maintain compliance with ICH E6(R2) Good Clinical Practice (GCP), FDA regulations, and institutional policies
  • Participate in study initiation meetings, protocol training, and ongoing sponsor communications
  • Support preparation for regulatory inspections and internal quality audits
  • Report adverse events and protocol deviations promptly and accurately per study requirements


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