Registered Nurse – Clinical Research Team
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
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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