Clinical Research Coordinator

USC Marshall School of Business; Huntington (WV); On-site; USD 52,000 - 72,000; Full time

Job summary

USC Marshall School of Business in Huntington, WV seeks a clinical support professional to assist physicians and investigators with PFT, hearing tests, injections, specimen collection, and study materials.

You will ensure timely communication of findings, maintain regulatory binders, and apply good clinical practice while using Microsoft Office and communicating with regulators and sponsors.

Qualifications

• Experience supporting clinical activities in a regulatory environment.
• Strong organizational skills and attention to detail.
• Proficiency with Microsoft Office Suite.

Responsibilities

• Collaborate with Clinical Activities – PFT, hearing, injections, specimen collection, and related tasks.
• Ensure timely communication of clinical findings/reports to appropriate agency or department and maintain regulatory materials.

Skills

Interpersonal skills

Organizational skills

Attention to detail

Microsoft Office

Tools

Microsoft Office Suite

Job description

Job Description

Job Responsibilities Collaborate with Clinical Activities – PFT , hearing, injections, specimen collection, etc. Clinical support for physician/investigator/clinical team; Ensure clinical findings/reports are communicated timely to proper agency/department; Support various clinical education and training requirements; Shows excellent interpersonal skills to deal effectively with clinicians, patients, administrators, auxiliary personnel, regulators, monitors, and sponsors; Understands and is knowledgeable of medical terminology, good clinical practice, FDA , OHRP , HIPAA policies; Experience with Microsoft Office Suite; Manages workflow independently with excellent organizational skills; Prioritizes quickly and appropriately with the ability to multi-task; Pays meticulous attention to detail Ability to review, understand, and apply complex protocols; Manages study materials including but not limited to, regulatory binders, study specific source documentation protocols training certification and other materials as required.