Travel Nurse Practitioner

ECN Operating LLC; Pasadena (CA); On-site; USD 120,000 - 160,000; Full time

Job summary

ECN Operating LLC in California seeks a Board-Certified Nurse Practitioner to join as Sub-Investigator for clinical research in Pomona, Northridge, and Pasadena. You will support the Principal Investigator in conducting trials while delivering high-quality care to study participants.

This role offers flexible hours, a collaborative environment, and comprehensive training. You will work directly with participants in a setting akin to a traditional clinical practice, contributing to protocol

Qualifications

• Licensed and board-certified NP required.
• Graduation from an accredited NP program.
• Current CPR and First Aid certification.
• GCP and Human Subjects Protection certification (or willingness to obtain).
• Prior clinical experience; research experience preferred.
• Strong attention to detail and team collaboration.

Responsibilities

• Conduct and document complete physical examinations of research participants.
• Review medical histories, labs, and diagnostic tests.
• Perform minor procedures including blood collection per protocol.
• Diagnose, assess, and treat study participants per protocols.
• Collaborate with PI and team to ensure GCP and regulatory compliance.
• Monitor participant safety and report adverse events.
• Maintain accurate study records in compliance with sponsor/regulatory requirements.

Skills

Attention to detail

Team collaboration

Clinical documentation

Education

Nurse Practitioner program graduate

Tools

GCP certification

Human Subjects Protection

Job description

Career Opportunities with ECN Operating LLC

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We are seeking a Board-Certified Nurse Practitioner to join our team as a Sub-Investigator for clinical research studies in Pomona, Northridge, and Pasadena. In this role, you will support the Principal Investigator in the conduct of clinical trials while providing high-quality care to study participants.

This position offers flexible hours, a collaborative work environment, and comprehensive training. You will work directly with research participants in a setting similar to a traditional clinical practice.

Responsibilities:

• Conduct and document complete physical examinations of research participants.
• Review medical histories, laboratory results, and diagnostic tests.
• Perform minor clinical procedures, including blood collection and other protocol-related assessments.
• Diagnose, assess, and treat study participants in alignment with study protocols.
• Collaborate with the Principal Investigator (PI) and clinical research team to ensure adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Monitor participant safety, report adverse events, and ensure proper documentation.
• Maintain accurate and timely study-related records in compliance with sponsor and regulatory requirements.

Qualifications:

• Licensed and Board-Certified Nurse Practitioner (required).
• Graduation from an accredited NP program.
• Current CPR and First Aid certification.
• Certification in Good Clinical Practice (GCP) and Human Subjects Protection (or willingness to obtain upon hire).
• Prior clinical experience (research experience preferred, but training provided).
• Strong attention to detail and ability to work collaboratively in a team-oriented environment.