Clinical Trials Coordinator — Patient-Centric Research

Highmark Health; Pittsburgh (Allegheny County); On-site; USD 65,000 - 90,000; Full time

Job summary

Highmark Health is seeking a Clinical Research Coordinator to plan, coordinate, and manage clinical trials across sponsored studies. You will ensure compliance with GCP, regulatory requirements, and study protocols while educating patients and families about participation and risks.

The role involves coordinating data collection, regulatory binder management, and ongoing monitoring to safeguard participant safety and data integrity in a dynamic hospital setting.

Qualifications

• Minimum Associate's degree, RN, or equivalent research experience.
• 1-3 years' related experience.
• Preferred Bachelor's Degree.
• Certification from AC RP/ SOCRA (CCRP) preferred.
• Driver's license may be required depending on facility requirements.

Responsibilities

• Identify patients eligible for clinical trials and interface with clinical staff.
• Provide in-service education to hospital personnel involved in the investigational study.
• Educate patients and families about investigational studies and participation requirements; obtain written consent and monitor per protocol.
• Collect, maintain, and store all relevant clinical data, case report forms, and regulatory binders.
• Plan, coordinate, and manage activities for clinical trials ensuring patient safety, GCP, and protocol/regulatory compliance.
• Perform other duties as assigned.

Skills

Clinical research coordination

Regulatory compliance

Patient education

Data collection

Education

Associate's degree, RN, or equivalent

Bachelor's degree preferred

Job description

Highmark Health is seeking a Clinical Research Coordinator to plan, coordinate, and manage clinical trials across sponsored studies. You will ensure compliance with GCP, regulatory requirements, and study protocols while educating patients and families about participation and risks.

The role involves coordinating data collection, regulatory binder management, and ongoing monitoring to safeguard participant safety and data integrity in a dynamic hospital setting.