Clinical Research Coordinator - Full Time - Wph - Oncology Research

Highmark Health

Unknown, Unknown, USA
Clinical trial initiation and completion
Patient and family education
Protocol and regulatory compliance
This job plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials

Job Summary

  • This job plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials.
  • Interfaces with patients and their families to provide education regarding investigational studies, and requirements of participation to assure that they are informed prior to obtaining written consent.
  • Collects, maintains, and stores all relevant clinical data, case report forms, and regulatory binders in accordance with the study sponsor and all regulatory bodies.

Matching Summary

This job plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials.

Skills & Requirements

Must-have

  • Clinical trial initiation and completion
  • Patient and family education
  • Protocol and regulatory compliance
  • Clinical data collection and maintenance

Nice-to-have

  • In-service education to hospital personnel
  • Active patient monitoring

Key Requirements

  • Associate's degree, RN, or equivalent research experience
  • 1-3 years’ related experience
  • Bachelor’s Degree (Preferred)
  • Current research-related certification (ACRP, SOCRA) (Preferred)
  • Driver's license may be required

Work Rights

Not specified

Tailored Resume

Cover Letter