Clinical Research Nurse

Tandem Intermediate LLC•Marrero, LA

About The Position

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.

Requirements

Bachelor’s degree required
Active Registered Nurse (RN) license required
Demonstrated competency in phlebotomy and infusion procedures
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 confidentiality
Proficiency with clinical and office equipment

Nice To Haves

Prior experience as a Clinical Research Coordinator, Research Assistant, or Clinical Research Nurse preferred
Phlebotomy and infusion experience required

Responsibilities

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.
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.
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.
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.
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.
Maintain timely, accurate clinical source documentation.
Support monitor visits and respond to clinical clarification requests.
Ensure documentation meets protocol, sponsor, and regulatory standards.
Responsibilities may expand based on protocol requirements, clinic operations, and organizational needs. Flexibility and collaboration are essential to success in this role.