Clinical Research Coordinator - Trial Ops & Patient Care

ochsner

New Orleans (LA)

On-site

USD 52,000 - 78,000

Full time

3 days ago
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Job summary

Ochsner Health in New Orleans, LA, is seeking a Clinical Research Coordinator to evaluate, initiate, and maintain activities related to clinical trials. You will coordinate trials, communicate with sponsors, and manage patient care requirements.

The role requires at least 3 years of clinical research experience (or 2 years with ACRP/SOCRA), and a current BLS certification. You’ll work in a dynamic environment with adherence to Good Clinical Practice guidelines.

Qualifications

  • Knowledge of medical and clinical research terminology and processes.
  • Working knowledge of ICH guidelines for ethical conduct of research.
  • Strong critical thinking skills.

Responsibilities

  • Organizes strategies for recruiting study participants and screening participants for eligibility.
  • Coordinates and oversees patient activity related to clinical trials and acts as liaison for patient and PI.
  • Serves as primary contact for patients to report adverse events and conducts informed consent.
  • Arranges necessary tests and procedures per protocol and reports results to the investigator.
  • Performs clinical laboratory activities as required per protocol and maintains study supplies and equipment.
  • Maintains documentation related to conduct of clinical trials and patient care.
  • Completes data entry into sponsor systems and supports data coordinators.
  • Adheres to Good Clinical Practice guidelines in daily work.

Skills

Medical terminology
ICH guidelines
Critical thinking
Budget development
Epic experience

Education

High school diploma

Tools

Epic

Job description

Ochsner Health in New Orleans, LA, is seeking a Clinical Research Coordinator to evaluate, initiate, and maintain activities related to clinical trials. You will coordinate trials, communicate with sponsors, and manage patient care requirements.

The role requires at least 3 years of clinical research experience (or 2 years with ACRP/SOCRA), and a current BLS certification. You’ll work in a dynamic environment with adherence to Good Clinical Practice guidelines.

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