On-Site Neuroscience Clinical Trials Coordinator

Ochsner Health; New Orleans (LA); On-site; USD 52,000 - 76,000; Full time

Job summary

Ochsner Health in New Orleans is seeking a Clinical Trials Coordinator to evaluate, initiate, and maintain activities related to the conduct of clinical trials. You will coordinate patient care requirements, communicate with sponsors, and support all phases of trial management.

Required: high school diploma and 3 years of clinical research experience or 2 years with ACRP/SOCRA certification; current BLS in AHA.

Qualifications

• Knowledge of medical and clinical research terminology and processes.
• Ability to follow and provide critical feedback on the investigational plan.
• Proficiency in using computers and software, including Epic.

Responsibilities

• Organizes strategies for recruiting study participants and screening eligibility.
• Coordinates and oversees patient activity related to trials and acts as liaison for PI.
• Triages adverse events and conducts informed consent.
• Arranges tests and procedures per protocol and reports results.
• Maintains documentation and supplies for trials.
• Communicates with sponsor representatives for initiation and close-out of studies.
• Performs data entry and supports data coordination.

Skills

Strong communication

Attention to detail

Time management

Team collaboration

Education

High school diploma or equivalent

Tools

Epic

Job description

Ochsner Health in New Orleans is seeking a Clinical Trials Coordinator to evaluate, initiate, and maintain activities related to the conduct of clinical trials. You will coordinate patient care requirements, communicate with sponsors, and support all phases of trial management.

Required: high school diploma and 3 years of clinical research experience or 2 years with ACRP/SOCRA certification; current BLS in AHA.