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Clinical Research Registered Nurse (RN)
Job Location:
Job Location:
West Hollywood, CA - USA
Monthly Salary:
Not provided by the employer
Monthly Salary:
Posted:
10 June 2026 (30+ days ago)
Posted:
Application Deadline:
7 September 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Position: Clinical Research Registered Nurse (RN)
Location: West Hollywood CA 90046
Location: West Hollywood CA 90046
Overview:
The Clinical Research Registered Nurse (RN) plays a critical role in the successful execution of clinical trials. This position combines clinical nursing practice with research operations to ensure the safe compliant and efficient conduct of studies while delivering high-quality patient-centered care.
The Clinical Research Registered Nurse (RN) plays a critical role in the successful execution of clinical trials. This position combines clinical nursing practice with research operations to ensure the safe compliant and efficient conduct of studies while delivering high-quality patient-centered care.
The RN is responsible for performing protocol-specific procedures supporting participant recruitment and retention administering investigational products and ensuring accurate and timely documentation of clinical and research data. This role works closely with investigators research coordinators and clinical operations leadership to support study implementation and ongoing trial conduct.
The Clinical Research RN maintains strict adherence to study protocols Good Clinical Practice (GCP) International Council for Harmonisation (ICH) guidelines HIPAA FDA regulations and all applicable state and local requirements.
Key Responsibilities:
Clinical Research Activities
Clinical Research Activities
- Perform protocol-required clinical procedures including physical assessments specimen collection phlebotomy injections IV placement and administration and preparation/administration of investigational products.
- Ensure accurate timely and complete documentation in source documents electronic health records and case report forms (CRFs/eCRFs).
- Support participant recruitment screening and enrollment by reviewing medical records and assessing eligibility criteria.
- Obtain and document informed consent in compliance with regulatory and ethical standards.
- Monitor participant safety by reviewing laboratory results performing medication reconciliation and identifying/reporting adverse events.
- Dispense investigational products according to protocol requirements and maintain appropriate documentation.
- Collect process handle and ship biological specimens while maintaining specimen integrity and chain of custody.
Compliance & Quality
- Maintain compliance with study protocols GCP SOPs HIPAA FDA regulations and applicable regulatory requirements.
- Participate in monitoring visits audits sponsor communications and quality assurance activities.
- Support corrective and preventive actions as needed.
- Maintain a safe and compliant clinical environment by following infection-control and safety procedures.
Participant Care & Education
- Provide patient-centered care in a respectful and non-judgmental manner.
- Educate participants regarding study procedures investigational treatments and follow-up requirements.
- Promote participant engagement retention and protocol adherence.
Team Collaboration
- Collaborate with investigators clinical research coordinators laboratory staff providers and sponsor representatives.
- Participate in team meetings protocol trainings and ongoing educational activities.
- Provide cross-functional support to research and clinical teams as needed.
- Assist with inventory management of clinical and research supplies.
Qualifications:
Required
Required
- Active Registered Nurse (RN) license in the State of California.
- Current Basic Life Support (BLS) certification.
- Prior clinical trial/research experience.
- Excellent interpersonal and communication skills.
- Strong attention to detail.
Preferred
- Minimum of three (3) years of direct patient care experience.
- Experience in HIV/AIDS treatment prevention or infectious disease research.
- Knowledge of state and federal reporting requirements related to infectious diseases.
Skills & Competencies:
- Strong clinical assessment and critical-thinking skills.
- Knowledge of clinical research regulations and Good Clinical Practice (GCP).
- Ability to manage multiple priorities in a fast-paced research environment.
- Strong documentation and organizational skills.
- Ability to work effectively with diverse patient populations and multidisciplinary teams.
- Understanding of psychosocial behavioral and motivational factors that impact patient health and research participation.
