PART-TIME
Posted Nov 4, 2026
Job Description
Position Summary
ECN Clinical is seeking a compassionate and detail-oriented IV Infusion Registered Nurse to assist our clinical research site team. This role offers a unique opportunity to contribute to groundbreaking research studies across multiple therapeutic areas. Whether you're experienced in research or transitioning from a clinical setting, we provide supplemental training to help you succeed in this exciting field.
Key Responsibilities
• Conduct physical exams and clinical assessments on study participants per protocol.
• Review laboratory results, ECGs, and other clinical findings and report abnormalities to the Principal Investigator.
• Assist with medication administration, including injections and infusions when required by study protocol.
• Collect vital signs, medical histories, and other baseline information as needed for clinical trial documentation.
• Maintain accurate and timely documentation in source documents and electronic data capture (EDC) systems.
• Collaborate with study coordinators, investigators, and other research staff to ensure compliance with protocols, GCP, and regulatory standards.
• Assist in maintaining study supplies and investigational product accountability.
• Participate in monitoring visits, audits, and site initiation or close-out visits as necessary.
• Ensure patient safety and comfort, identifying and escalating any adverse events or deviations.
Qualifications
• Active Registered Nurse (RN) license.
• Minimum of 1 year of nursing experience (clinical or research setting).
• IV Infusion experience (IV starts, maintenance, and medication administration).
• Strong understanding of clinical procedures, vital sign collection, and patient monitoring.
• Excellent communication, organizational, and multitasking skills.
• Ability to work independently and as part of a multidisciplinary team.
• Basic computer proficiency including Microsoft Office and familiarity with EMRs or EDC systems.
Preferred Experience (Not Required)
• Prior experience in clinical research, pharma trials, or investigational drug studies.
• Knowledge of ICH-GCP guidelines and FDA regulations.
• Familiarity with clinical trial protocols and informed consent procedures.
• BLS certification
Additional Position Details
• Temporary Contract
• Per Diem/Part-Time weekly schedule
• Competitive hourly compensation based on experience
Pay
• $55-60/hour
ECN Clinical is seeking a compassionate and detail-oriented IV Infusion Registered Nurse to assist our clinical research site team. This role offers a unique opportunity to contribute to groundbreaking research studies across multiple therapeutic areas. Whether you're experienced in research or transitioning from a clinical setting, we provide supplemental training to help you succeed in this exciting field.
Key Responsibilities
• Conduct physical exams and clinical assessments on study participants per protocol.
• Review laboratory results, ECGs, and other clinical findings and report abnormalities to the Principal Investigator.
• Assist with medication administration, including injections and infusions when required by study protocol.
• Collect vital signs, medical histories, and other baseline information as needed for clinical trial documentation.
• Maintain accurate and timely documentation in source documents and electronic data capture (EDC) systems.
• Collaborate with study coordinators, investigators, and other research staff to ensure compliance with protocols, GCP, and regulatory standards.
• Assist in maintaining study supplies and investigational product accountability.
• Participate in monitoring visits, audits, and site initiation or close-out visits as necessary.
• Ensure patient safety and comfort, identifying and escalating any adverse events or deviations.
Qualifications
• Active Registered Nurse (RN) license.
• Minimum of 1 year of nursing experience (clinical or research setting).
• IV Infusion experience (IV starts, maintenance, and medication administration).
• Strong understanding of clinical procedures, vital sign collection, and patient monitoring.
• Excellent communication, organizational, and multitasking skills.
• Ability to work independently and as part of a multidisciplinary team.
• Basic computer proficiency including Microsoft Office and familiarity with EMRs or EDC systems.
Preferred Experience (Not Required)
• Prior experience in clinical research, pharma trials, or investigational drug studies.
• Knowledge of ICH-GCP guidelines and FDA regulations.
• Familiarity with clinical trial protocols and informed consent procedures.
• BLS certification
Additional Position Details
• Temporary Contract
• Per Diem/Part-Time weekly schedule
• Competitive hourly compensation based on experience
Pay
• $55-60/hour
Additional Details
- City
- San Jose
- State
- California
- Country
- US
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