Clinical Research Nurse

Tandem Clinical Research, LLC; Marrero (LA); On-site; USD 65,000 - 85,000; Full time

Job summary

Tandem Clinical Research, LLC is seeking a Clinical Research Nurse to perform protocol-required nursing and clinical procedures for assigned studies. You will work closely with the Principal Investigator, Sub-Investigators, and Clinical Research Coordinators to ensure patient safety, high-quality clinical execution, and compliance with study protocols and regulatory standards.

As the primary owner of licensed nursing care, you will conduct clinical assessments, phlebotomy, infusion

Qualifications

• Bachelor’s degree and active RN license are required.
• Experience as Clinical Research Coordinator or similar preferred.
• Phlebotomy and infusion skills are required.

Responsibilities

• Perform protocol-required nursing procedures, including vitals, ECGs, phlebotomy, and infusions.
• Assess patients, monitor adverse events, and escalate concerns.
• Educate patients about study participation and procedures.
• Maintain accurate source documentation and data integrity.
• Collaborate with investigators, coordinators, sponsors, and monitors.

Skills

Verbal communication

Written communication

Interpersonal skills

Patient care

Multi-office environment

Organizational skills

Attention to detail

Confidentiality

Equipment proficiency

Phlebotomy and infusion

Education

Bachelor's degree

RN license

Job 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 clarification 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 & Qualifications

• 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