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HACKENSACK UNIVERSITY MED CNTR

Sr Clinical Data Coordinator

Pay: Not specified

Posted: 3 weeks ago

Location: Hackensack, NJ (Onsite)

Last Updated: 1 week ago

Hours: Full-Time

Expires: 9/29/2026

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What they do

A Clinical Data Coordinator reviews data collected for a clinical trial and coordinates administrative tasks and records related to the trial. Manages clinical trial software and databases and creates reports. May coordinate data collection for different clinical trial sites.

$72,819 / year median in New Jersey

+23% projected growth

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Job Description

Our team members are the heart of what makes us better. At Hackensack Meridian Health we help our patients live better, healthier lives — and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. It's also about how we support one another and how we show up for our community. Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change The Sr. Clinical Data Coordinator is responsible for the oversight of the data management process for their respective division(s) or assignments. This includes, but is not limited to, data entry, query management, and ensuring adherence to institutional and protocol requirements while maintaining data integrity for all assigned clinical research studies.

Qualifications:

Education, Knowledge, Skills and Abilities Required:

BA/BS diploma/degree in science or healthcare field OR minimum of 4 or more years of experience in a related area with High School diploma, general equivalency diploma (GED), and/or GED equivalent programs. Strong attention to detail and customer service focus. 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). If you feel the above description speaks directly to your strengths and capabilities, then please apply today!