Clinical Research Coordinator - Organized Trials & Docs

LCMC Health; New Orleans (LA); Sur place; USD 45 000 - 70 000; Plein temps

Résumé du poste

LCMC Health in New Orleans, LA coordinates clinical trials across planning, enrollment, and ongoing activities to ensure compliant, timely study execution. You’ll develop timelines, manage trial plans, and handle regulatory submissions while maintaining precise source documentation and supplier tracking.

In this role, you’ll communicate with sponsors, participants, and clinical teams to keep studies on track, protect privacy, and support regulatory compliance.

Qualifications

• Bachelor’s Degree in a related field.
• 2+ years of experience in post-graduate medical education and medical research studies.

Responsabilités

• Coordinate clinical trials from planning through ongoing activities.
• Review study requirements and help develop timelines, workflows, and trial plans.
• Support participant enrollment and follow-up visits.
• Complete case report forms and maintain source documentation.
• Track investigational meds, devices, and study supplies.
• Prepare and submit regulatory documents and study correspondence.
• Organize research workflows, records, and trial documentation.
• Communicate with study sponsors, participants, and internal teams.
• Troubleshoot operational issues to keep studies on protocol.

Connaissances

Organizational skills

Time-management

Communication

Interpersonal abilities

Attention to detail

Computer literacy

Documentation

Sponsor coordination

Formation

Bachelor’s Degree in a related field

Outils

ECG machines

Spirometers

Stadiometers

Scales

Description du poste

LCMC Health in New Orleans, LA coordinates clinical trials across planning, enrollment, and ongoing activities to ensure compliant, timely study execution. You’ll develop timelines, manage trial plans, and handle regulatory submissions while maintaining precise source documentation and supplier tracking.

In this role, you’ll communicate with sponsors, participants, and clinical teams to keep studies on track, protect privacy, and support regulatory compliance.