Clinical Research Coordinator - Full Time - Wph - Oncology Research

Highmark Health

Pittsburgh, PA, US
Patient safety
Good clinical practices
Regulatory compliance
This job plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials, sponsored by internal, industry, foundation, and/or Federal funding sources

Job Summary

  • This job plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials, sponsored by internal, industry, foundation, and/or Federal funding sources.
  • 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, sponsored by internal, industry, foundation, and/or Federal funding sources.

Skills & Requirements

Must-have

  • patient safety
  • good clinical practices
  • regulatory compliance
  • patient education
  • data collection and maintenance

Nice-to-have

  • in-service education
  • patient and family engagement
  • protocol adherence

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter