Clinical Research Coordinator: Impactful Trials & Patients

Ochsner Health; New Orleans (LA); On-site; USD 55,000 - 75,000; Full time

Job summary

Ochsner Health in New Orleans seeks a clinical research support professional to evaluate, initiate, and maintain clinical trial activities under supervision. You will coordinate patient care, consent processes, and protocol-required procedures while ensuring data integrity and regulatory compliance.

The role requires knowledge of clinical research terminology, ICH guidelines, and Epic proficiency, with strong organizational and communication skills.

Qualifications

• Knowledge of medical and clinical research terminology.
• Familiarity with ICH guidelines for ethical conduct of research.
• Ability to follow the investigational plan in execution of study visits.
• Strong organizational and time management skills.
• Knowledge of regulatory requirements for clinical trials.
• Proficiency with Epic and related data systems.
• Effective verbal and written communication skills.
• Willingness to travel between facilities and maintain flexible schedule.

Responsibilities

• Assist in recruiting and screening study participants.
• Coordinate patient activity related to research and clinical trials.
• Arrange tests/procedures per protocol requirements.
• Perform clinical laboratory activities as required by protocol.
• Develop and maintain trial documentation and sponsor data entries.
• Ensure compliance with Good Clinical Practice guidelines.
• Adapt interactions to patient population and privacy needs.
• Perform additional duties as assigned.

Skills

Medical terminology

ICH guidelines

Investigational plan

Organizational skills

Regulatory knowledge

Epic proficiency

Verbal and written communication

Travel flexibility

Education

High school diploma or equivalent

Bachelor's degree in life science

Tools

Epic

Job description

Ochsner Health in New Orleans seeks a clinical research support professional to evaluate, initiate, and maintain clinical trial activities under supervision. You will coordinate patient care, consent processes, and protocol-required procedures while ensuring data integrity and regulatory compliance.

The role requires knowledge of clinical research terminology, ICH guidelines, and Epic proficiency, with strong organizational and communication skills.