Senior Trauma Clinical Data Coordinator - Full Time - Day

Hackensack Meridian Health Inc.; Hackensack (NJ); On-site; USD 75,000 - 105,000; Full time

Job summary

Hackensack Meridian Health Inc. is seeking a Senior Trauma Clinical Data Coordinator to oversee data management for the Department of Trauma at Hackensack University Medical Center.

You will handle research data entry, query management, and ensure protocol adherence while maintaining data integrity for all Trauma studies. In this role you will support the Trauma Program under the Trauma Research Nurse Coordinator, Trauma Program Manager and Chief of Trauma to help maintain Level 1 Trauma ACS

Qualifications

• Bachelor’s degree in science or healthcare or 4+ years related experience with HS/GED.
• Strong attention to detail and organizational skills.
• Advanced knowledge of medical terminology and EPIC EMR.
• Excellent written and verbal communication.

Responsibilities

• Oversee data management for the Department of Trauma at HUMC.
• Handle research data entry, query management, and protocol adherence.
• Support Trauma Program to maintain Level 1 Trauma ACS Certification.

Skills

Attention to detail

Medical terminology

EPIC EMR

Organizational skills

Communication skills

Office/Google Suite

Education

Bachelor's degree in science or healthcare

4+ years related experience with HS/GED

Tools

EPIC

Job description

The Senior Trauma Clinical Data Coordinator is responsible for the oversight of the data management for the Department of Trauma at Hackensack University Medical Center (HUMC). This includes, but is not limited to, research related data entry, query management, and ensuring adherence to institutional and protocol requirements while maintaining data integrity for all assigned Trauma clinical research studies. This role also supports the Trauma Program under the direction of the Trauma Research Nurse Coordinator, Trauma Program Manager and Chief of Trauma to ensure that Level 1 Trauma ACS Certification is maintained.

Education, Knowledge, Skills and Abilities Required:

• Bachelor of Arts/Bachelor of Science diploma/degree in science or healthcare field OR minimum of 4+ years of experience in a related area with High School diploma, general equivalency diploma (GED), and/or GED equivalent programs.
• Strong attention to detail.
• Advanced knowledge in Medical Terminology.
• Advanced/Expert knowledge in electronic medical record (EPIC).
• Ability to work independently, or in a team, and handle multiple deadline driven tasks in a dynamic environment is essential.
• Excellent organizational, presentation, documentation and interpersonal skills.
• Excellent written and verbal communication skills.
• Proficient computer skills that include but are not limited to Microsoft Office and/or Google Suite platforms.

Education, Knowledge, Skills and Abilities Preferred:

• Minimum of 4 or more years of extensive experience in research that includes data abstracting, case report form completion and research regulatory reporting.
• Education on human subject research and GCP.

Licenses and Certifications Preferred:

• SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC).