Clinical Research Nurse

Tandem Intermediate LLC; Marrero (LA); On-site; USD 70,000 - 90,000; Full time

Job summary

Tandem Intermediate LLC is seeking a Clinical Research Nurse to perform protocol-required nursing procedures and patient monitoring in clinical trials. You will collaborate with the Principal Investigator, Sub-Investigators, and Clinical Research Coordinators to ensure subject safety and protocol compliance.

Responsibilities include phlebotomy, infusion administration, vital signs, ECGs, specimen handling, and maintaining accurate source documentation.

Qualifications

• Bachelor’s degree required.
• Active RN license required.
• Experience as a Clinical Research Coordinator, Research Assistant, or Clinical Research Nurse preferred.
• Phlebotomy and infusion experience required.

Responsibilities

• Perform protocol-required nursing and clinical procedures, including vitals, ECGs, phlebotomy, infusions, specimen handling, and documentation.
• Monitor subjects before, during, and after procedures for safety and protocol compliance.
• Maintain timely, accurate clinical source documentation and support monitor visits.

Skills

Verbal & written communication

Interpersonal skills

Patient care

Fast-paced environment

Organization

Attention to detail

Confidentiality

Clinical equipment

Phlebotomy

Infusion procedures

Education

Bachelor’s degree

RN license

Job description

Description

The Clinical Research Nurse is responsible for performing protocol-required nursing and clinical procedures for assigned research studies. This role works in close collaboration with the Principal Investigator, Sub-Investigators, and Clinical Research Coordinators to ensure subject safety, high-quality clinical execution, and compliance with study protocols and regulatory standards.

The Clinical Research Nurse serves as the primary owner of licensed nursing care, clinical assessments, phlebotomy, infusion administration, and patient monitoring within clinical trials.

Key Responsibilities

Study & Protocol Knowledge

• Maintain thorough knowledge of assigned studies through protocol review, investigator meetings, start-up meetings, and collaboration with the Principal Investigator.
• Adhere strictly to study protocols, GCP, and regulatory requirements.
• Obtain protocol exemptions or deviations when appropriate and approved.

Clinical & Nursing Procedures

• Perform protocol-required nursing and clinical procedures, including but not limited to:
• Vital signs, height, and weight
• ECGs
• Phlebotomy and specimen collection
• Preparation, administration, and monitoring of infusions, as required by protocol and within scope of licensure
• Specimen processing, packaging, and shipment
• Monitor subjects before, during, and after procedures to ensure safety and protocol compliance.
• Dispense investigational products and maintain accurate administration documentation, as applicable.

Patient Assessment & Safety

• Collect initial and ongoing medical and psychiatric information through patient interviews and record review.
• Assess and monitor adverse events and clinical changes.
• Escalate safety concerns and clinical issues to the Principal Investigator and study team promptly.

Patient Education & Support

• Educate patients and families regarding study participation, investigational products, and clinical trial processes.
• Ensure patient understanding of procedures, risks, and expectations.
• Provide appropriate community referrals at the conclusion of study participation.

Communication & Collaboration

• Maintain clear communication with patients, investigators, CRCs, sponsors, CROs, monitors, and auditors.
• Participate in meetings and calls related to clinical execution.
• Support multi-site collaboration when applicable.

Documentation & Data Integrity

• Maintain timely, accurate clinical source documentation.
• Support monitor visits and respond to clinical clari?cation requests.
• Ensure documentation meets protocol, sponsor, and regulatory standards.

Additional Responsibilities

This job description outlines the primary responsibilities of the Clinical Research Nurse but is not intended to be exhaustive. Responsibilities may expand based on protocol requirements, clinic operations, and organizational needs. Flexibility and collaboration are essential to success in this role.

Requirements

Knowledge, Skills, and Abilities

• Strong verbal and written communication skills
• Excellent interpersonal and patient-care skills
• Ability to work effectively in a fast-paced, multi-office environment
• Strong organizational and multitasking abilities
• High attention to detail and commitment to patient safety
• Ability to maintain con?dentiality
• Pro?ciency with clinical and office equipment
• Demonstrated competency in phlebotomy and infusion procedures

Required Experience & Quali?cations

• Education: Bachelor’s degree required
• Licensure: Active Registered Nurse (RN) license required
• Experience: Prior experience as a Clinical Research Coordinator, Research Assistant, or Clinical Research Nurse preferred
• Clinical Skills: Phlebotomy and infusion experience required