Nurse Practitioner

Elite Clinical Network; San Diego (CA); On-site; USD 83,000 - 117,000; Full time

Job summary

Elite Clinical Network seeks a Board-Certified Nurse Practitioner to join as a Sub-Investigator for clinical research studies in San Diego, CA. You will support the Principal Investigator in conducting trials and provide high-quality care to participants.

The role offers flexible hours, a collaborative environment, and comprehensive training. You will work directly with research participants in a setting similar to a traditional clinical practice and ensure adherence to study protocols, GCP, and

Qualifications

• Must be a licensed and board-certified Nurse Practitioner.
• 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 on hire).
• Active DEA registration preferred, but not required.
• Prior clinical/research experience; training provided.

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.
• Administer and/or dispense investigational products per protocol with licensed oversight.
• Diagnose, assess, and treat study participants per study protocol.
• Collaborate with the PI and clinical research team to ensure GCP adherence and regulatory compliance.
• Monitor participant safety, report adverse events, and maintain proper documentation.
• Maintain accurate study-related records in compliance with sponsor and regulatory requirements.

Skills

Board-Certified NP

Licensed NP

CPR & First Aid

GCP & Human Subjects Protection

Research experience

Attention to detail

Team collaboration

Willingness to obtain GCP

Education

Master of Science in Nursing (NP program)

Job description

Job Overview

We are seeking a Board-Certified Nurse Practitioner to join our team as a Sub-Investigator for clinical research studies. 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.
• Administer and/or dispense investigational products, including injections, infusions, and other protocol-required therapies requiring an appropriately licensed healthcare professional, in accordance with study protocols and applicable regulations.
• 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).
• Active DEA registration preferred, but not required.
• Prior clinical experience (research experience preferred, but training provided).
• Strong attention to detail and ability to work collaboratively in a team-oriented environment.

Pay

• $60-85/hr