Clinical Research Coordinator — Critical Care & Trauma Trials

University-of-North-Carolina-At-Chapel-Hil; Chapel Hill (NC); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

Professional training opportunities

Exclusive perks for discounts

Health, life and retirement plan perks

Job summary

The University of North Carolina at Chapel Hill is seeking a Clinical Research Coordinator within the Critical Care and Trauma Research Unit in the Department of Surgery. The role involves planning, organizing, and conducting multiple clinical research study protocols, including consenting and data collection.

You will ensure compliance with protocols, regulatory requirements, and Good Clinical Practice guidelines, maintain meticulous study documents, and report adverse events.

Qualifications

• Bachelor’s degree in a discipline related to the field and one year of related training or experience.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Experience coordinating clinical research studies and data management tasks preferred.

Responsibilities

• Plan, organize and conduct multiple clinical research protocols, including consenting and data collection.
• Ensure trial activities follow study protocols, regulatory requirements and GCP; maintain study documents and report adverse events.
• Specialize in extracorporeal purification device, wound healing, and pharmacokinetic/pharmacodynamic trials.

Skills

Clinical research coordination

Data collection

Data management

Regulatory compliance

GCP guidelines

Stakeholder communication

Education

Bachelor’s degree in a related field

Job description

The University of North Carolina at Chapel Hill is seeking a Clinical Research Coordinator within the Critical Care and Trauma Research Unit in the Department of Surgery. The role involves planning, organizing, and conducting multiple clinical research study protocols, including consenting and data collection.

You will ensure compliance with protocols, regulatory requirements, and Good Clinical Practice guidelines, maintain meticulous study documents, and report adverse events.